A-A-53049
Unit.
For Size 1 – Package (PG). Shall be supplied in a vial containing 30 ml. One package containing 25 vials, as specified, constitutes one unit.
For Size 2 - Shall be supplied in a vial containing 50 ml. One package containing 25 vials, as specified, constitutes one unit.
For Size 3, Type I – Bottle (BT). One bottle containing 300 ml, as specified, constitutes one unit. Shall be supplied without an infusion set.
For Size 3, Type II - Package (PG). Shall be supplied in bottle containing 300 ml. One package containing one bottle together with one infusion set, as specified, constitutes one unit.
Contractor certification. The contractor shall certify that the product offered meets the salient characteristics of this description and conforms to the producers’ own drawings, specifications, standards, and quality assurance practices. The Government reserves the right to require proof of such conformance prior to first delivery and thereafter as may be otherwise provided for under the provisions of the contract.
Regulatory requirements.
Federal Food, Drug and Cosmetic Act. If the product covered by this document has been determined by the U.S. Food and Drug Administration to be under its jurisdiction, the offeror/contractor shall comply, and be responsible for compliance by its subcontractors/suppliers, with the requirements of Federal Food, Drug and Cosmetic Act, as amended, and regulations promulgated thereunder. In addition, the offeror/contractor shall comply, and be responsible for compliance by its subcontractors/suppliers, with the requirements of all other applicable Federal, State, and local statutes, ordinances, and regulations.
Recovered materials. The offeror/contractor is encouraged to use recovered materials in accordance with Public Law 94-580 to the maximum extent practical.
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