Exhibit 2.1
ASSET PURCHASE
AGREEMENT
by and between
MERIT MEDICAL SYSTEMS,
INC.
and
HATCH MEDICAL,
L.L.C.
June 2, 2009
Table of
Contents
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1.
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Definitions
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1
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2.
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Basic Transactions
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5
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(a)
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Transactions
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5
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(b)
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Assumption/Exclusion of
Liabilities
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5
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(c)
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Consideration Provided by Buyer for
Acquired Assets
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5
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(d)
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Allocation of Purchase
Price
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6
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(e)
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The Closing
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6
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(f)
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Deliveries at the Closing
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6
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3.
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Representations and Warranties of
Sellers
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6
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(a)
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Organization of Seller
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6
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(b)
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Authorization of
Transaction
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6
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(c)
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Noncontravention
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7
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(d)
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Title to Assets; Sufficiency of
Assets
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7
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(e)
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No Adverse Change
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7
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(f)
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Legal Compliance
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7
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(g)
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Intellectual Property
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8
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(h)
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Environmental, Health, and Safety
Matters
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10
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(i)
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Contracts
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11
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(j)
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Litigation
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12
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(k)
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Product Warranty
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12
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(l)
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Product Liability
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12
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(m)
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Customers and Suppliers
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12
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(n)
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Pre-Closing
Representations
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12
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(o)
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Broker Fees
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13
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(p)
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Disclaimer
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13
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4.
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Representations and Warranties of
Buyer
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13
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(a)
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Organization of Buyer
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13
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(b)
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Authorization of
Transaction
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13
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(c)
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Noncontravention
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13
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(d)
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Brokers’ Fees
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13
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(e)
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Financial Status
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13
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i
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5.
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Conditions to
Closing
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13
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(a)
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Conditions to Obligation of
Buyer
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13
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(b)
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Conditions to Obligation of
Sellers
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15
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6.
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Pre-Closing
Covenants
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16
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(a)
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General
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16
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(b)
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Notices and Consents
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16
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(c)
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Operation of Business
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16
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(d)
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Full Access
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17
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(e)
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Notice of Developments
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17
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(f)
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No Participation or Solicitation of
Competing Transaction
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17
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(g)
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Completion of Non-assignable
Agreements
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17
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(h)
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Royalty Payments
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17
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7.
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Post-Closing
Covenants
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18
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(a)
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General
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18
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(b)
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Litigation Support
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18
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(c)
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Confidentiality
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18
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(d)
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Transfer of Assets
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19
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8.
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Remedies for Breaches of this
Agreement
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20
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(a)
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Survival of Representations and
Warranties
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20
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(b)
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Indemnification Provisions for
Benefit of Buyer and Sellers
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20
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(c)
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Matters Involving Third
Parties
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21
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(d)
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Characterization of
Payments
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22
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(e)
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Limitations
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22
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(f)
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Exclusive
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23
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9.
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Termination
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23
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(a)
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Termination of Agreement
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23
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(b)
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Effect of Termination
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23
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10.
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Miscellaneous
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23
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(a)
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Press Releases and Public
Announcements
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23
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(b)
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No Third-Party
Beneficiaries
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23
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(c)
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Entire Agreement
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23
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(d)
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Succession and Assignment
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23
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(e)
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Counterparts
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24
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ii
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(f)
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Headings
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24
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(g)
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Notices
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24
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(h)
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Governing Law;
Jurisdiction
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25
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(i)
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Amendments and Waivers
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25
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(j)
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Severability
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25
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(k)
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Expenses
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25
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(l)
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Construction
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25
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(m)
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Incorporation of Exhibits and
Schedules
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26
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(n)
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Specific Performance
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26
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(o)
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Waiver of Trial By Jury
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26
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(p)
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Transfer Taxes
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26
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Exhibit A
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Allocation of the Purchase
Price
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Exhibit B
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Bill of Sale
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Exhibit C
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Assignment and Assumption of
Acquired Contracts
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Exhibit D
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Intellectual Property Transfer
Documents
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Exhibit E
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Non-Competition Agreement
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Exhibit F
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Form of Opinion of
Seller’s Counsel
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Exhibit G
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Form of Opinion of
Buyer’s Counsel
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Disclosure Schedule
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Exceptions to Representations and
Warranties of Seller
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iii
ASSET PURCHASE
AGREEMENT
This Asset Purchase Agreement (this
“Agreement”) is entered into as of June 2, 2009,
by and between Merit Medical Systems, Inc., a Utah corporation
(“Buyer”) and Hatch Medical, L.L.C., a Georgia limited
liability company (“Seller”). Buyer and Seller
are referred to collectively herein as the “Parties”
and individually as a “Party.”
RECITALS
A.
Seller owns the intellectual
property and other assets related to a certain medical device
described as a “Foreign Body Retrieval System” and
known as the EnSnare® device (the
“Device”).
B.
Seller desires to sell the Device
and other assets related thereto to Buyer, and Buyer desires to
purchase such assets from Seller, in exchange for the consideration
set forth herein, all upon the terms and subject to the conditions
of this Agreement.
C.
Seller and Buyer are willing to make
certain representations, warranties, covenants and agreements in
connection with such sale and purchase.
AGREEMENT
NOW, THEREFORE, in consideration of
the premises and the mutual promises herein made, and in
consideration of the representations, warranties, and covenants
herein contained, the Parties agree as follows:
1.
Definitions . For purposes of this
Agreement, the following terms have the meanings set forth
below:
“Acquired Assets” means
each of the following, as of the Closing Date (a) all Acquired
Intellectual Property; (b) the EnSnare In-Vivo Evaluation
— Final Report dated May 1, 2002 (the “Animal
Study”); (c) plans, drawings and specifications, and all
books, records and files, related to the Acquired Intellectual
Property which Seller either owns or both possesses and has the
right to assign to Buyer, Seller; (d) to the extent in the
possession of Seller, any vendor and supplier lists related to the
Device; (e) all goodwill of Seller related exclusively to the
Acquired Assets; (f) the Acquired Contracts; (g) all
tangible and intangible property received by Seller from Angiotech
(as defined in the definition of License Agreement), which Seller
either owns or both possesses and has the right to assign to Buyer,
whether pursuant to the terms of the License Agreement or otherwise
related to the Device, at any time before or after the Closing (and
if received after Closing, to be delivered to Buyer promptly
following Seller’s receipt thereof); and (h) any plans,
drawings and specifications, and all books, records and files,
related to the Neuro line extension or the clot capturing line
extension which Seller either owns or both possesses and has the
right to assign to Buyer.
“Acquired Contracts”
means the contracts, leases, licenses and other agreements or
arrangements of Seller related exclusively to the Device which are
listed on Schedule 1(a) attached hereto.
“Acquisition Proposal”
shall mean any proposal or offer made by any Person other than the
Buyer or any Affiliate thereof to acquire, license, distribute,
market, manufacture, lease or transfer all or any part of, the
Device or any of the Acquired Assets (or any of Seller’s
interest in the Device or any of the Acquired Assets), or to enter
into a transaction outside of the Ordinary Course of Business
affecting the Device or any of the Acquired Assets.
1
“Adverse Consequences”
means all damages, dues, penalties, fines, costs, amounts paid in
settlement, obligations, taxes, Encumbrances, losses or fees,
together with all reasonable expenses and fees, including without
limitation court costs and attorneys’ fees and expenses,
arising out of any actions, suits, proceedings, hearings, official
inquiries, investigations, charges, complaints, claims, demands,
injunctions, judgments, orders, decrees or rulings.
“Acquired Intellectual
Property” means the following Intellectual
Property:
(a)
all inventions
(whether patentable or unpatentable, whether or not reduced to
practice, and whether or not the subject of any patent
applications) and any additions and improvements thereto which
Seller either owns or both possesses and has the right to assign to
Buyer, comprising or related to the Device and necessary in the
manufacture or distribution of the Device;
(b)
all patents,
patent rights, patent disclosures, utility models, certificates of
invention, statutory invention registrations, and applications for
any of the foregoing, together with any reissuances, continuations,
continuations in part, revisions, extensions, divisions, renewals,
or reexaminations of any of the foregoing, all as listed on
Section 3(g)(iii) of the Disclosure Schedule (each a
“Patent”);
(c)
all trademarks,
service marks, trade dress, logos, trade names listed on
Section 3(g)(iii) of the Disclosure Schedule, together
with any translations, adaptations, derivations, and combinations
thereof and including all goodwill associated therewith, and any
applications, registrations, and renewals in connection therewith
(each, a “Trademark”);
(d)
all works of
authorship which Seller either owns or both possesses and has the
right to assign to Buyer listed on Section 3(g)(iii) of
the Disclosure Schedule in whatever form or medium, any copyrights
therein (whether registered or unregistered), and any applications,
registrations, and renewals relating thereto (each, a
“Copyright”);
(e)
all trade secrets
and Confidential Information which Seller either owns or both
possesses and has the right to assign to Buyer related to the
Device and necessary or desirable in the manufacture or
distribution of the Device, including but not limited to ideas,
research and development, know-how, formulas, processes, protocol,
compositions, manufacturing and production processes and
techniques, procedures, devices, technical data, designs, drawings,
specifications and supplier lists;
(f)
all other
proprietary rights in information and technology which Seller
either owns or both possesses and has the right to assign to Buyer
related to the Device and necessary in the manufacture or
distribution of the Device, including without limitation the Animal
Study;
(g)
all copies and
tangible embodiments of any of the foregoing in whatever form or
medium;
(h)
all legal and
equitable remedies for past, present, and future infringements,
misappropriations, misuses, dilutions, and other violations of any
of the foregoing, subject to the rights of Angiotech under the
License Agreement;
(i)
all other
Intellectual Property related to the Neuro line extension or the
clot capturing line extension which Seller either owns or both
possesses and has the right to assign to Buyer; and
2
(j)
all rights,
title, and interests in and to any of the foregoing provided by any
treaty, statute, convention, common law, regulation, or any other
Law.
“Affiliate” has the
meaning set forth in Rule 12b-2 of Regulation 12B promulgated
under the Securities Exchange Act.
“Assumed Liabilities”
shall have the meaning set forth in
Section 2(b)(i) below.
“Closing” has the
meaning set forth in Section 2(f) below.
“Closing Date” has the
meaning set forth in Section 2(f) below.
“Confidential
Information” means any information regarding the business and
affairs of Seller or Buyer that is not generally available to the
public on the date hereto. Information that may be included
in Confidential Information includes, but is not limited to,
matters of a technical nature (including Intellectual Property,
know-how, computer programs, software, patented and unpatented
technology, source-code, accounting methods, and documentation),
matters of a business nature (such as information regarding
contract forms, costs, profits, employees, promotional methods,
markets, market or marketing plans, sales, and client accounts),
plans for further development, and any other information meeting
the definition of Confidential Information set forth
above.
“Disclosure Schedule”
has the meaning set forth in Section 3 below.
“Encumbrance” shall mean
any mortgage, pledge, assessment, security interest, deed of trust,
lease, lien, adverse claim, levy, charge or other encumbrance of
any kind, or any conditional sale or title retention agreement or
other agreement to give any of the foregoing in the
future.
“Excluded Liabilities”
shall have the meaning set forth in
Section 2(b)(ii) below.
“Governmental Authority”
means any government, state, commonwealth or any subdivision
thereof, whether domestic, foreign or multinational, or any agency,
authority, bureau, commission, department or similar body or
instrumentality thereof, or any governmental court or tribunal, and
any self-regulatory agency, industry group or other governing body
or authority.
“Indemnified Party” has
the meaning set forth in Section 8(c) below.
“Indemnifying Party” has
the meaning set forth in Section 8(c) below.
“Intellectual Property”
means (a) inventions (whether patentable or
unpatentable, whether or not reduced to practice, and whether or
not the subject of any patent applications) and any additions and
improvements thereto; (b) patents, patent rights, patent
disclosures, utility models, certificates of invention, statutory
invention registrations, and applications for any of the foregoing,
together with any reissuances, continuations, continuations in
part, revisions, extensions, divisions, renewals, or reexaminations
of any of the foregoing (each a “Patent”),
(c) trademarks, service marks, trade dress, logos, trade
names, Internet domain names and URLs, and corporate names,
together with any translations, adaptations, derivations, and
combinations thereof and including all goodwill associated
therewith, and any applications, registrations, and renewals in
connection therewith (each, a “Trademark”);
(d) works of authorship in whatever form or medium, any
copyrights therein (whether registered or unregistered), and any
applications, registrations, and renewals relating thereto (each, a
“Copyright”); (e) trade secrets and Confidential
Information, including but not limited to ideas, research and
development, know-how, formulas, processes, protocol, compositions,
manufacturing and production
3
processes and techniques,
sterilization processes and validation information, procedures,
devices, technical data, designs, drawings, specifications,
customer and supplier lists, pricing and cost information, and
business and marketing plans and proposals; (f) mask works;
(g) any other proprietary rights in information and
technology, including without limitation any pre-clinical and
clinical data and information; (h) copies and tangible
embodiments of any of the foregoing in whatever form or medium;
(i) legal and equitable remedies for past, present, and future
infringements, misappropriations, misuses, dilutions, and other
violations of any of the foregoing; and (j) rights, title, and
interests in and to any of the foregoing provided by any treaty,
statute, convention, common law, regulation, or any other
Law.
“Laws” means all
federal, state, municipal, foreign, and international laws, rules,
regulations, codes, statutes, constitutions, ordinances,
directives, treaties, proclamations, conventions, and orders, and
all judicial, quasi-judicial and administrative and other official
interpretations of any of the foregoing.
“Liability” means any
liability, obligation, debt, demand, claim, expense or commitment
(whether known or unknown, whether asserted or unasserted, whether
absolute or contingent, whether accrued or unaccrued, whether
liquidated or unliquidated, and whether due or to become
due).
“License Agreement”
means that certain License Agreement, dated October 2, 2001
and as amended by that certain Amendment to License Agreement dated
December 17, 2004, between Seller and Angiotech
Pharmaceuticals, Inc., as successor or assignee to Medical
Device Technologies, Inc.
(“Angiotech”).
“Material Adverse
Effect” means an effect or effects which, individually or in
the aggregate, (i) with respect to Seller, materially affects
the Seller’s ability to consummate the Transactions, or could
reasonably have an adverse economic effect on the Acquired Assets
or Device of $100,000 or more, or (ii) with respect to Buyer,
an effect or effects which, individually or in the aggregate,
materially affects Buyer’s ability to consummate the
Transactions.
“Ordinary Course of
Business” means the ordinary course of business consistent
with past custom and practice (including with respect to quantity,
frequency and price).
“Person” means an
individual, a partnership, a limited liability company, limited
partnership, a limited liability partnership, a corporation, an
association, a joint stock company, a trust, a joint venture, an
unincorporated organization, or a Governmental
Authority.
“Purchase Price” has the
meaning set forth in Section 2(c) below.
“Securities Exchange
Act” means the Securities Exchange Act of 1934, as
amended.
“Seller’s
knowledge” is applicable to certain of those warranties and
representations set forth in Section 3 of this Agreement or
other provisions elsewhere in this Agreement, which are subject to
the qualification “to Seller’s knowledge” or
“to the knowledge of Seller,” or otherwise limited to
matters “known” to Seller. Seller will be deemed
to have “knowledge” of a matter relating to Seller, the
Device or the Acquired Assets if an executive officer of Seller had
knowledge of such matter or would have acquired such knowledge had
he or she inquired at or prior to that time as to such subject
matter to those of Seller’s employees that would be expected
to have knowledge of such subject matter in the course of
performing their duties for Seller. Seller will be deemed to
have “knowledge” of a matter relating to a third party
only if an executive officer of Seller had actual knowledge of such
matter (except as otherwise set forth above in this
definition).
“Third Party Claim” has
the meaning set forth in
Section 8(c)(i) below.
4
“Transaction Documents”
means this Agreement and the agreements, documents, schedules,
letters or certificates attached hereto as an Exhibit or
delivered pursuant to this Agreement or in connection with the
Transactions.
“Transactions” means the
transactions provided for or contemplated by this Agreement and the
other Transaction Documents.
2.
Basic Transactions
.
(a)
Transactions
. On and
subject to the terms and conditions of this Agreement, Buyer agrees
to purchase from Seller, and Seller agrees to sell, transfer,
convey, assign and deliver to Buyer, title to and ownership of, all
of the Acquired Assets at the Closing, for the consideration
specified below in this Section 2. Title to the Acquired
Assets shall pass to Buyer at the Closing, and risk of loss shall
pass to Buyer upon receipt by Buyer of the Acquired Assets.
The Parties intend for all of the Acquired Assets to be transferred
to Buyer, whether owned by Seller, an Affiliate of Seller or
otherwise, and Seller agrees to cause all of the Acquired Assets to
be sold, transferred, conveyed, assigned and delivered to Buyer in
accordance with the terms of this Agreement. The parties
acknowledge and agree that the Acquired Assets do not include the
assets described on Schedule 2(a) (the “Excluded
Assets”).
(b)
Assumption/Exclusion of
Liabilities .
(i)
Assumed
Liabilities . Subject to the
conditions specified in this Agreement, on the Closing Date, Buyer
will assume and agree to pay, defend, discharge and perform as and
when due only the liabilities and obligations under the Acquired
Contracts (“Assumed Liabilities”) arising or accruing
only after the Closing Date, but only to the extent that
Seller’s rights and benefits under such Acquired Contracts
are validly assigned to Buyer pursuant to this Agreement.
Buyer shall also be solely responsible for, and shall pay and
perform, all obligations and liabilities resulting from or arising
out of the ownership or use of the Acquired Assets solely after the
Closing Date (“Post-Closing Liabilities”).
(ii)
Excluded
Liabilities . Notwithstanding
anything to the contrary contained in this Agreement, Buyer will
not assume or be liable for, and will have no responsibility
related to, any Liabilities of Seller of any kind or nature, other
than the Assumed Liabilities (all such Liabilities collectively,
the “Excluded Liabilities”). Seller retains sole
liability for all Excluded Liabilities.
(c)
Consideration
Provided by Buyer for the Acquired Assets . Subject to the terms
and conditions of this Agreement, including, without limitation,
the provisions of Section 2(d) below, as total
consideration for the Acquired Assets, Buyer shall pay Seller an
aggregate of Twenty-One Million Dollars ($21,000,000) (the
“Purchase Price”), as follows:
(i)
(A) Buyer
shall deliver to Seller at the Closing, by wire transfer in
accordance with Seller’s wiring instructions, Fourteen
Million Dollars ($14,000,000) less the escrowed amounts held
pursuant to the Escrow Agreement among Buyer, Seller and Zions
First National Bank, as escrow agent (“Zions”), and
(B) Zions shall deliver to Seller at Closing, by wire transfer
in accordance with Seller’s wiring instructions, all escrowed
amounts held pursuant to such Escrow Agreement; and
(ii)
Buyer shall pay
to Seller Seven Million Dollars ($7,000,000) upon the later of the
following: (A) three (3) business days after the date
upon which Buyer has completed manufacturing of the first unit of
the Device for commercial sale (with respect to which Buyer shall
use all commercially reasonable efforts in good faith to complete
all matters necessary to be in a position to
5
perform such
manufacturing as soon as possible after the date set forth in the
following clause (B)), or (B) the earlier of December 31,
2009 or the date upon which all third-party contractual rights
(including, without limitation, under the License Agreement) with
respect to manufacturing, marketing and distributing of the Device
have finally expired or terminated.
(d)
Allocation of
Purchase Price . The Purchase Price
shall be allocated among the Acquired Assets as set forth on
Exhibit A attached hereto and made a part hereof.
Buyer will allocate the Purchase Price among the Acquired Assets in
a reasonable manner in accordance with Section 1060 of the
Internal Revenue Code and the regulations thereunder, based on the
relative fair market values of the Acquired Assets, which Buyer
shall complete and deliver to Seller within 90 days following the
Closing. In the event that Seller reasonably disagrees with
the proposed allocation, the Parties will work and negotiate in
good faith to resolve any disputes and finalize such allocation as
soon as possible thereafter. Buyer and Seller will file all
of their tax returns consistent with the foregoing allocation and
will not take any position inconsistent with such allocation on any
tax return or in any tax audit or tax-related
proceeding.
(e)
The
Closing . The closing of the
transactions contemplated by this Agreement (the
“Closing”) shall take place at the offices of the
Buyer, commencing at 10:00 a.m. local time on the second
business day following the satisfaction or waiver of all conditions
to the obligations of the Parties to consummate the Transactions
(other than conditions with respect to actions the respective
Parties will take at the Closing itself) or such other date, time
and place as Buyer and Seller may mutually determine (the
“Closing Date”). The Parties shall use
commercially reasonable efforts to cause the Closing to occur
within five (5) business days from the date
hereof.
(f)
Deliveries at
the Closing . At the Closing,
(i) Seller will deliver to Buyer (or cause its Affiliates to
deliver to Buyer) the various certificates, instruments, and
documents referred to in Section 5(a) below;
(ii) Buyer will deliver to Seller the various certificates,
instruments, and documents referred to in
Section 5(b) below; and (iii) Buyer will deliver to
Seller the consideration specified in
Section 2(c)(i) above. The Parties also acknowledge
the obligations and matters set forth in Section 7 of this
Agreement.
3.
Representations and Warranties of
Seller . Except as otherwise
set forth in the disclosure schedule delivered by Seller to Buyer
on the date hereof (the “Disclosure Schedule”), Seller
represents and warrants to Buyer on the date hereof and on the
Closing Date (as though made on the Closing Date and as though the
Closing Date were substituted for the date of this Agreement
throughout this Section 3) as follows:
(a)
Organization
of Seller . Seller is a limited
liability company duly organized, validly existing and in good
standing under the laws of Georgia. Seller has full limited
liability company power and authority to carry on the business in
which it is engaged, and to own and use the properties owned and
used by it.
(b)
Authorization
of Transaction . Seller has full
limited liability company power and authority to execute and
deliver this Agreement and the Transaction Documents to which it is
a party and to perform its obligations hereunder and
thereunder. The execution, delivery and performance of this
Agreement and the Transaction Documents by Seller and the
consummation of the Transactions have been duly and validly
authorized by all necessary limited liability company action on the
part of Seller and no other proceedings on the part of Seller are
necessary to authorize this Agreement or any of the Transaction
Documents or to consummate any of the Transactions. This
Agreement and the other Transaction Documents to which Seller is a
party, assuming the due authorization, execution and delivery
hereof and thereof by Buyer hereto and thereto, constitute the
valid and legally binding obligations of
6
Seller, as
applicable, enforceable against Seller in accordance with their
terms and conditions, except as enforceability may be limited by
applicable bankruptcy, insolvency or similar laws affecting or
relating to the enforcement of creditors’ rights generally or
by equitable principles relating to enforceability.
(c)
Non-contravention
. Neither
the execution and delivery of this Agreement nor any of the other
Transaction Documents to which Seller is a party, nor the
consummation of the Transactions, will (i) violate any Law or
other restriction of any Governmental Authority to which Seller is
subject or any provision of the articles of organization or
operating agreement (or any other governance document) of Seller or
(ii) conflict with, result in a breach of, constitute a
default under, result in the acceleration of, create in any party
the right to accelerate, terminate, modify, or cancel, or require
any notice under any agreement, contract, lease, license,
instrument, or other arrangement to which Seller is a party or by
which it is bound or to which any of the Acquired Assets is subject
(or result in the imposition of any Encumbrance upon any of the
Acquired Assets), or (iii) require Seller to obtain or make
any waiver, consent, action, approval or authorization of, or
registration, declaration, notice or filing with, any Governmental
Authority or private non-governmental third-party.
Section 3(c) of the Disclosure Schedule sets forth each
consent required from a third party (including any Governmental
Authority) in order for Seller to consummate the Transactions
(including to sell and assign the Acquired Assets to Buyer free and
clear of any Encumbrance) or where such consent is required by the
terms of an Assumed Contract or other Acquired Assets.
(d)
Title to
Assets; Sufficiency of Assets . Seller owns, and has
good and marketable title to, all of the Acquired Assets, free and
clear of any Encumbrance or other restriction on transfer, other
than the Assumed Liabilities. At the Closing, Seller will
convey to Buyer good and marketable title to all of the Acquired
Assets, free and clear of any Encumbrance or other restriction on
transfer. The Acquired Assets include all assets and rights
necessary (other than regulatory approvals) for Buyer to build
equipment to manufacture the Device, and, following such building,
to then sell, distribute and market the Device commercially and
exercise all rights of ownership of the Device (following
expiration of Angiotech’s rights under
Section 13(c) of the License Agreement). Following
the Closing, but subject to Angiotech’s rights under
Section 13(c) of the License Agreement, Buyer will own
and possess all rights necessary (other than regulatory approvals)
to commercially manufacture, sell, distribute, market and license
the Device.
(e)
No Adverse
Change . Except as set forth
on Section 3(e) of the Disclosure Schedule, since
January 1, 2008, there has not been any Material Adverse
Effect on the business, financial condition, operations, results of
operations, or future prospects of Seller with respect to the
business of the Device or the Acquired Assets. Without
limiting the generality of the foregoing, since that date, with
respect to the Device:
(i)
Seller has not
sold, leased, transferred, or assigned any of the Acquired
Assets;
(ii)
Seller has not
granted any license or sublicense or any rights under or with
respect to any Acquired Intellectual Property;
(iii)
Seller has not
committed to any of the foregoing; and
(iv)
Seller has not
experienced any damage, destruction, or loss (whether or not
covered by insurance) to its tangible Acquired Assets.
(f)
Legal
Compliance . Seller and each of
its predecessors and Affiliates has complied with all applicable
Laws of any Governmental Authority related to the Acquired Assets,
except
7
for violations
which, in the aggregate, could not reasonably be expected to have a
Material Adverse Effect. Seller has not received any written
notice or other communication from any Governmental Authority
regarding any actual or potential violation of, or failure to
comply with, any applicable Laws, as the same related to the
Acquired Assets, and no action, suit, proceeding, hearing,
investigation, charge, complaint, claim, demand, or notice has been
filed or commenced against Seller or any of its predecessors or
Affiliates alleging any failure to so comply.
(g)
Intellectual
Property .
(i)
Seller owns all
Acquired Intellectual Property, subject to the rights licensed
under the License Agreement. Seller has taken all necessary
action to maintain and protect its rights in each item of Acquired
Intellectual Property, and the confidentiality of each such item,
except where a failure to do so would not have a Material Adverse
Effect. Seller has no knowledge of any information,
materials, facts or circumstances, including any information or
fact that would constitute prior art, that would render any
Acquired Intellectual Property invalid or
unenforceable.
(ii)
The Device, as it
has previously been or is currently being manufactured and sold,
does not infringe upon, misappropriate, misuse, dilute or otherwise
violate any Intellectual Property rights of any Person; the
creation and development of the Device did not infringe upon,
misappropriate, misuse, dilute or otherwise violate any
Intellectual Property right of any Person; and none of the officers
or directors (or employees with responsibility for Intellectual
Property matters) of Seller has ever received, or has knowledge of,
any charge, complaint, claim, allegation, demand, or notice,
whether directed to Seller, MD Tech, or to any MD Tech
subcontractor, sublicensee, subdistributor, or retailer, alleging
any such infringement, misappropriation, misuse, dilution or other
violation of any Person’s Intellectual Property (including
any claim that Seller, MD Tech, or any MD Tech subcontractor,
sublicensee, subdistributor, or retailer must license or refrain
from using any Intellectual Property of any Person). None of the
Acquired Intellectual Property infringes upon, misappropriates,
misuses, dilutes, or otherwise violates any Intellectual Property
rights of any Person. The Seller has no knowledge that any
Person is infringing upon, misappropriating, misusing, diluting, or
otherwise violating any Acquired Intellectual Property.
Except for the Excluded Assets, the Acquired Intellectual Property
includes all Intellectual Property necessary to manufacture, sell
or license, distribute, or market the Device in the manner that the
Device is currently being manufactured, sold or licensed,
distributed, or marketed commercially.
(iii)
Section 3(g)(iii) of
the Disclosure Schedule identifies each Patent, Copyright
registration, Trademark registration and other certificate and
registration that has been issued to Seller or any Affiliate of
Seller or any other Person with respect to any of the Acquired
Intellectual Property, identifies each pending application for a
Patent, Copyright registration, Trademark registration, and other
certificate and registration that Seller or any other Person has
made with respect to any of the Acquired Intellectual Property, and
identifies each license, sublicense, agreement, and other
permission which Seller has granted to any Person with respect to
any of the Acquired Intellectual Property (together with any
exceptions). Seller has delivered to Buyer correct and
complete copies of all such Patents, Copyright registrations,
Trademark registrations, other certificates, registrations,
applications, licenses, sublicenses, agreements, and permissions
(as amended to date) and has made available to Buyer correct and
complete copies of all other written documentation evidencing
ownership and prosecution (if applicable) of each such item.
With respect to each item of Intellectual Property required to be
identified in Section 3(g)(iii) of the Disclosure
Schedule:
(A)
Seller possesses
all right, title, and interest in and to the item, free and clear
of any Encumbrance, license, other restriction, or viable claims of
ownership by any Person, except
8
for such
licenses, agreements, and other permissions that Seller has granted
to any Person with respect to such item and that also are
identified in Section 3(g)(iii) of the Disclosure
Schedule;
(B)
the item is not
subject to any binding outstanding injunction, judgment, order,
decree, or other ruling of any Governmental Authority of competent
jurisdiction;
(C)
the item was
validly acquired under applicable Laws and remains valid,
enforceable, and subsisting;
(D)
no action, suit,
proceeding, hearing, investigation, charge, complaint, claim,
allegation or demand has been initiated is pending or, to
Seller’s best knowledge, is threatened that challenges the
legality, validity, enforceability, use, or ownership of the
item;
(E)
Seller has no
agreement or obligation to indemnify any Person for or against any
infringement, misappropriation, misuse, dilution, or other
violation with respect to the item, except for agreements entered
into with suppliers or customers in the Ordinary Course of
Business; and
(F)
Seller has not
committed any act or omission that would result in the abandonment,
cancellation, forfeiture, relinquishment, invalidation or
unenforceability of the item, and no information, facts or
circumstances would otherwise render the item invalid or
unenforceable.
(iv)
Section 3(g)(iv) of
the Disclosure Schedule identifies each item of Acquired
Intellectual Property that any Person owns and that Seller uses
pursuant to license, sublicense, agreement, or permission (other
than off-the-shelf software with a purchase or license price of
less than $10,000). Seller has delivered to Buyer correct and
complete copies of all such licenses, sublicenses, agreements, and
permissions (as amended to date). With respect to each item
of Acquired Intellectual Property required to be identified in
Section 3(g)(iv) of the Disclosure Schedule:
(A)
the license,
sublicense, agreement, or permission covering the item is legal,
valid, binding, enforceable, and in full force and
effect;
(B)
the consummation
of the Transactions and the Parties’ performance as required
under the Transaction Documents will not affect the respective
license’s, sublicense’s, agreement’s, or
permission’s legality, validity, binding nature,
enforceability, or existence, and the same shall remain in full
force and effect on identical terms once assigned to
Buyer;
(C)
the Seller is not
in breach or default of, and to the best knowledge of the Seller no
other party is in breach or default of, any license, sublicense,
agreement, or permission, and no event has occurred, relating to
Seller or to Seller’s knowledge related to a third party,
that with notice or lapse of time would constitute a breach or
default or permit termination, modification, or acceleration
thereunder;
(D)
the Seller has no
knowledge that any party to a license, sublicense, agreement, or
permission has informed any other party thereto that it repudiates
any provision thereof;
(E)
with respect to
each sublicense, the representations and warranties set forth in
subsections (A) through (D) above are true and correct
with respect to the underlying license;
(F)
the underlying
item of Intellectual Property is not subject to any outstanding
injunction, judgment, order, decree, or other ruling of any
Governmental Authority of competent jurisdiction;
9
(G)
no action, suit,
proceeding, hearing, investigation, charge, complaint, claim, or
demand has been initiated to which Seller is a party, is pending,
or is threatened against Seller that challenges the legality,
validity, enforceability, use or ownership of the underlying item
of Acquired Intellectual Property; to Seller’s knowledge, no
action, suit, proceeding, hearing, investigation, charge,
complaint, claim, or demand has been initiated, or is pending or
has been threatened against any third party that challenges the
legality, validity, enforceability, use or ownership of the
underlying item of Acquired Intellectual Property;
(H)
Seller has not
granted any sublicense or similar right with respect to such
license, sublicense, agreement, or permission; and
(I)
No information,
facts, or circumstances exist that would render the underlying item
of Intellectual Property invalid or unenforceable.
(v)
Except as set
forth on Section 3(g)(v) of the Disclosure Schedule, all
of the employees of Seller have entered into invention assignment
and confidentiality agreements under which such employees have
assigned to Seller all of their right, title and interest in and to
Intellectual Property related to the Acquired Intellectual Property
and agreed not to use or disclose, other than for the benefit of
Seller or its successors or assigns, any Confidential Information
of Seller that is included in the Acquired Intellectual
Property. Except as set forth on Section 3(g)(v) of
the Disclosure Schedule, all independent contractors and
consultants of Seller who participated in the conception, creation,
reduction to practice, or other development of any Acquired
Intellectual Property has entered into invention assignment and
confidentiality agreements under which such contractors and
consultants have assigned to Seller all of their right, title and
interest in and to Intellectual Property related to the Acquired
Intellectual Property and have agreed not to use or disclose, other
than for the benefit of Seller or its successors or assigns, any
Confidential Information of Seller that is included in the Acquired
Intellectual Property. To Seller’s knowledge, no such
employee, independent contractor or consultant has breached any of
the provisions of any such agreement.
(vi)
Seller has
undertaken its best efforts to protect and enforce its rights in
all Acquired Intellectual Property and, to Seller’s
knowledge, MD Tech has undertaken its best efforts to protect and
enforce the Patents that are the subject of the License
Agreement.
(vii)
Except as set
forth on Section 3(g)(vii) of the Disclosure Schedule, no
filing, response, or payment must be made, within ninety (90) days
after the Closing Date, for Seller to perfect, prosecute, protect,
maintain, or renew its rights in or to any item of Acquired
Intellectual Property.
(viii)
Notwithstanding
the foregoing, the parties agree that representations and
warranties contained in this Section 3(g) shall not apply
to the Intellectual Property related to the Neuro line extension or
the clot capturing line extension.
(h)
Environmental,
Health, and Safety Matters . Seller and its
predecessors and Affiliates have complied with all applicable
environmental, health, and safety Laws the failure of which to
comply with would have an adverse effect on the Acquired Assets or
which could create any Encumbrance on the Acquired Assets.
Without limiting the generality of the foregoing, Seller and its
predecessors and Affiliates has obtained and complied with all
permits, certificates, licenses, filings, approvals and other
authorizations of any Governmental Authority that are required
pursuant to any applicable environmental, health, and
safety
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