A-A-51774A
For Strength I, the injection shall be suitable for nerve block infiltration.
For Strength II, the injection shall be suitable for caudal and epidural blocks.
For Strength IV, the injection shall be suitable for local anesthetic for dental block and filtration injections. Shall be paraben-free.
All ingredients entering into the manufacture of the injection shall be a pharmaceutical grade.
Workmanship. The injection shall be free from defects which detract from ite appearance or impair its serviceability.
Unit.
Package (PG).
For Size 1, shall be supplied 1.8 ml in a clear Type I USP glass cartridge. One package containing 100 cartridges, as specified, constitutes one unit.
Vial (VI).
For Size 2, shall be supplied 20 ml in a commercially available multiple dose vial. One vial, as specified, constitutes one unit.
For Size 3, shall be supplied 30 ml in a commercially available single dose vial. One vial, as specified, constitutes one unit.
For Size 4, shall be supplied 50 ml in a commercially available multiple dose vial. One vial, 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.
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