[*] designates portions of this document that have been omitted pursuant to a request for confidential treatment
filed separately with the Securities and Exchange Commission.
MEDICAL SUPPLY MANUFACTURING AGREEMENT
THIS MEDICAL SUPPLY MANUFACTURING AGREEMENT (this “Agreement”) is made and
entered into as of 14 July 2010 between (i) MedPro Safety Products, Inc., a Nevada corporation (“MedPro”),
and Greiner Bio-One GmbH, an Austrian company (“GBO”).
WHEREAS, MedPro owns the following intellectual property rights:
VACUETTE® PREMIUM Safety Needle System (the “Tube-Activated Product” and the
“Skin-Activated Product”). The Tube-Activated Product and the Skin-Activated Product are referred to
hereinafter as the “Holder Product”, and
VACUETTE® PREMIUM Safety Blood Collection Set (PSBC) hereinafter referred to as the
“Wing Product”, and
Collectively the Holder Product and the Wing Product are herein referred to as the “Products”.
WHEREAS, MedPro wishes to grant, and GBO wishes to accept, the right to manuf acture and
distribute the Products, all in accordance with the terms and conditions of this Agreement.
WHEREAS, MedPro and GBO are parties to two agreements, titled ‘Medical Supply Manufacturing
Agreement’ and dated as of July 15
, 2008 and wish to terminate such agreements and supersede and replace
them with this consolidated and single Agreement.
NOW THEREFORE, in consideration of the mutual covenants and agreements contained herein,
MedPro and GBO agree as follows:
ARTICLE 1 - TERM AND PROCEDURES
1.1 Medical Supply Manufacturing Agreement. The two Medical Supply Manufacturing
Agreements for the products covered by this Agreement are hereby terminated effective as of the date first set
forth above, shall be of no further force or effect whatsoever, and are replaced and superseded in their entirety
by this Agreement.
1.2 Exclusive Rights . During the Term (as hereafter defined),