A-A-51823A
Type II. Type II tubes shall have two black lines, the outside edges of which are .197 in. apart. The end of the farthest line shall be 1.969 in. form one end of the tube. Tubes shall be coated internally with acridine orange, potassium oxalate, sodium heparin, K2 EDTA, agglutinating agent and stabilizers.
Float. Shall be a solid plastic cylinder having a density of 1.080 g/cm3 at 250C shall have an outside diameter of 0.06285 ± .00035 inches.
Tube closure. Shall be a cap suitable for fitting over one end of the tube. Shall have friction fit and form a leakproof seal to allow proper sampling for centrifugal hematology values.
Workmanship. The tube shall be free from defects which detract from their appearance or impair its serviceability.
Unit. Package (PG). One package containing one hundred centrifugal hematology tubes, as specified, constitutes one unit.
Quality Assurance Provisions.
Responsibility for inspection. Unless otherwise specified in the contract or purchase order, the contractor is responsible for the performance of all inspection requirements as specified herein. Except as otherwise specified in the contact or purchase order, the contractor may use his own or any facilities suitable for the performance of the inspection requirements specified herein, unless disapproved by the Government. The Government reserves the right to perform any of the inspections set forth in the specification where such inspections are deemed necessary to assure supplies and services conform to prescribed requirements.
Records. Records of examinations and tests performed by or for the contractor shall be maintained by the contractor and made available to the Government upon the Government’s request, at any time, or from time to time, during the performance of the contract and for a period of three years after delivery of the supplies to which such records relate.
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