1、A-A-54342 bb m 9999974 0059883 T m A-A-54342 4 February 1991 COMMERCIAL ITEM DESCRIPTION LOOP, INOCULATING, LABORATORY (Quantitative) The Geriei.al Ser%vicec: Administration has authorized the use of this Cominercial Item Description as a replacement for Military Specification MIL-L-37661 which was
2、cancel led. This Commercial Item Description covers a Breed type bacteriological inoculating loop that is quantitated to hold liquid inoculum. Shall be a Breed type bacteriological inoculating loop that is quantitated to hold 0.01 milliliter (ml1 of liquid i nocul um. Shall consist of a wire shank w
3、ith a loop at one end for holding a 0.01 ml sample. Shall-be fabricated of alloy having concentration of 3.5 percent rhodium and 96.5 percent platinum. Shall have a weight of not less than 0.90 grams. Shall have a nominal wire diameter size of 0.91 millimeters (mm) . Shall have a nominal length for
4、the shank of 50 mm. The nominal inside diameter of the loop shall be 4 mm. - Workmanship, The inoculating loop shall be free from defects which detract from its appearance or impair its serviceability. EnLi- Each (EA). One loop, as specified, constitutes one unit. AMSC N/A FSC 6640 QISTRIBUTION STAT
5、EMENT A: Approved for public release; distribution is unlimited. I Provided by IHSNot for ResaleNo reproduction or networking permitted without license from IHS-,-,-A-A-54342 66 S 9999974 O059884 L Rswponsibility-for insgsctioc, Unless otherwise specified in the contract or purchase order, the contr
6、actor is responsible for the performance of all inspection requirements as specified herein. Except as otherwise specified in the contract or purchase order, the contractor may use his own or any facilities suitable for the performance of the inspection requirements specified herein, unless disappro
7、ved 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, ggcoibg2 Records of examinations and tests performed by or for the
8、 contractor shall be maintained by the contractor and made available to the Uovernment upon the dovernments 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. - InsEections. -
9、 Inspections, as used herein, is defined as both examination (such as visual or auditory investigation without the use of special laboratory appliances or procedures) and testing (determination by technical means of physical and chemical properties) of the item. - Insgections -_ and tests. Inspect
10、ions and tests shall be conductei in accoi-dance with commercial practice to determine compliance with specification requirements. _- Sampling -_ _- for inspections - and tests. Sampling for inspections and tests shall be conducted in accordance with I commercial practice. _-_-_-_- Contractor certif
11、ication. 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
12、 first delivery and thereafter as may be otherwise provided for under the provisions of the contract. 2 I i i Provided by IHSNot for ResaleNo reproduction or networking permitted without license from IHS-,-,-A-A-54342 bb E 999997I 0059885 3 E A-A-54342 Federal Food,-Dyyg and Cosmetic Act. If the pro
13、duct covered bv this document has been determined by the U.S. Food and Drug Administration to be under its jurisdiction, offeror/contractor shall comply, and be responsible for compliance by its subcontractors/suppliers, with the requirements of the Federal Food, Drug and Cosmetic Act, as amended, a
14、nd 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. the Rgmxgred msigrigls- The offer
15、or/contractor is encouraged to use recovered material in accordance with Federal Acquisition Regulation Subpart 23.4 to the maximum extent practical. Un 1 sha rreserati-r_ea-kag-akg-g-g ess otherwise specified, preservation, packaging, and packing .ll be to a degree of protection to preclude damage
16、to containers and/or contents thereof under normal shipping conditions, handling, etc., involving shipment from the supply source to the receiving activity, plus reshipment from receiving activity, and shall conform to applicable carriers rules and regulations. Intermediate and exterior package quan
17、tities and labeling and marking shall be as specified in the contract and/or order. grdering-data. (Intermediate/exterior package quantities, labeling, and marking must be specified in the contract and/or order. 1 , NOTE: The following National Stock Number is covered by this document. 6640-01-025-3
18、176 LOOP, INOCULATIN(3, LABORATORY Quantitative, 0.01 ml. MILITARY INTERESTS: PREPARINC3 ACTIVITY: Custodians: DoD-MB Army - MD Navy - MS Air Force - 03 Agent: DLA-DM I- l 3 Provided by IHSNot for ResaleNo reproduction or networking permitted without license from IHS-,-,-A-A-54342 CIVIL AGENCY COORDINATING ACTIVITIES: VA-OSS PHS FDA - MP Q AS Project Number: 6640-1696 Location: ENABLE/LOOPCID/S31 4 Provided by IHSNot for ResaleNo reproduction or networking permitted without license from IHS-,-,-
