A-A-51894C
Type:
I. Shall be suitable for intramuscular or intravenous administration
II. Shall be suitable for intermittent intravenous administration.
III. Shall be compatible with the following diluents containers: 6505-01-260-1237, 6505-01-260-1238, 6505-01-260-1239, 6505-01-260-1241, 6505-01-260-1242, and 6505-01-260-6715.
Workmanship. The product shall be clean, uniform in quality and free from foreign material or any other defects which detract from their appearance or impair its serviceability.
Unit. Package (PG).
For Size I – Shall be supplied in a vial. One package containing 10 vials, as specified, constitutes one unit.
For Size II - Shall be supplied in a vial. One package containing 25 vials, as specified, constitutes one unit.
For Size III – Shall be supplied in a bottle with a rated capacity of not less than 100 ml. Bottle shall be supplied with a suitable hanging device. For use in pharmacy intravenous programs. One package containing 6 bottles with hanging devices, as specified, constitutes one unit.
For Size IV – Shall be supplied in a single dose, sterile 15 ml glass vial, having a double lead screw thread designed to interlock with the inlet port of selected diluents containers. One package containing 25 vials, 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 producer’s 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.
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