DOD A-A-55708-1996 ROTATOR LABORATORY VARIABLE SPEED《实验室变速旋转体》.pdf
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1、A-A- 55708 9 August 1996 - COMMERCIAL ITEM DESCRIPTION ROTATOR, LABORATORY, Variable Speed . The.Genera1 Services Administration has authorized the use of this Commercial Item Description for all Federal Agencies. 1. SCOPE. This Commercial Item Description covers a portable variable speed platform r
2、otator for use in a variety of laboratory procedures. 2. SALIENT CHARACTERISTICS: 2.1 The unit shall be a portable, variable speed, platform rotator for use in a variety of laboratory procedures including standard serological procedures. 2.2 The unit shall consist of a base and a top mounted platfor
3、m. 2.3 The unit shall have the nominal dimensions of 12 inches Wide by 13 inches Deep by 6 inches High. 2.4 The unit shall be equipped with: 2.4.1 A solid state speed control for selecting speeds in a nominal range of 80-210 rpms. 2.4.2 A 0-30 minute timer and a selector switch for timed or continuo
4、us operation. Beneficial comments, recommendations, additions, deletions, clarifications; etc. and any other data which may be used to improve this document should be sent to: Defense Personnel Support Center, Directorate of Medical Materiel, ATTN: DPSC-MBP, 2800 South 20th Street, Philadelphia, PA
5、19145-0530, by letter or usina the self-addressed Standardization Document Improvement d )Proposal, (DD Form 1426) appearinq at the end of this document. 1 FSC 6640 AMSC N/A DISTRIBUTION STATEMENT A: Approved for public release; distribution is unlimited. Provided by IHSNot for ResaleNo reproduction
6、 or networking permitted without license from IHS-,-,-A-A-55708 9993974 0172844 638 A-A- 5 5 7 O 8 2.4.3 A rimmed platform that is padded with a material that prevents labware from sliding during operation. The platform shall have nominal dimensions of 13 inches by 13 inches. 2.5 Workmanship. The la
7、boratory rotator shall be free from defects which detract from its appearance or impair its serviceability. 2.6 Unit. Each (EA). One laboratory rotator as specified, constitutes one unit. Each unit shall be packaged in accordance with the requirements of ASTM D 3951. 3. REGULATORY REOUIREMENTS. 3.1
8、Federal Food, Druq, 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 t
9、he 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, ordinance
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