DOD A-A-54193-1990 PAD POST-SURGICAL-OBSTETRICAL BELTLESS POSTPARTUM OR POSTOPERATIVE《产后或手术后的带子外科助产衬垫》.pdf

1、 A-A-54193 65 m 999797L( 005b959 2 m A-A-5 4 19 3 1 July 1990 COMMERCIAL ITEM DESCRIPTION PAD, POST-SURGICAL-OBSTRETRICAL, BELTLESS, POSTPARTUM OR POSTOPERATIVE The General Services Administration has authorized the use of this Commercial Item Description. This commercial item description covers a p

2、ost-parturn, post- operative, beltless pad. Salient characteristics. Shall be a clean, beltless, extra absorbent pereneal pad having a minimum length of 13 inches and a minimuni width of 3 inches. The pad shall be suitable for post-partum patients and post-operative vaginaUrecta1 patients. The fille

3、r shall be absorbent cellulose fibers. The cellulose fibers (fluff) shall be bleached white chemical wood pulp which shall be relatively free from inipurities and foreign matter. Other extra absorbent fibers and bleached absorbent creped cellulose may be used in combination with the cellulose fibers

4、. The absorbent fibers shall be contained so that they shall not penetrate the pad covering. The entire filler shall be free of any water soluable coloring matter. The filler shall not bunch or separate during use. The pad shall be completely wrapped and completely sealed with a soft nonwoven polypr

5、opylene based fiber fabric with the fiber having a minimum denier of four. The filler shall be completely contained within the pad. The dry breaking strength of the nonwoven fabric cover shall be a minimum of 5 pounds in the machine direction and a minimum of 3 pounds in the cross direction when tes

6、ted by ASTM D2208-80. The minimum weight of the nonwoven fabric cover shall be 0.70 ounces per square yard. The side of the pad opposite the patient side shall contain a sheet of soft plastic just under the nonwoven fabric cover and the sheet of soft plastic shall be a barrier against strike-through

7、 drainage, AMSC/NA FSC 6510 DISTRIBUTION STATEMENT A. Approved for public release; 0 distribution is unlimited. Provided by IHSNot for ResaleNo reproduction or networking permitted without license from IHS-,-,-A-A-54 19 3 The soft plastic sheet shall run the full length and width of the pad and shal

8、l be fastened in place. The side of the pad opposite the patient side sha3.1 have a pressure sensitive adhesive stripfs) which shall run almost the entire length of the pad on the outside of the pad. adhesive strip(c1 shall hold the pad securely in place during use and the pads shall be easily detac

9、hed for ,dispocal, The adhesive area shall be protected by an easily removable paper: facing. The The finished pad shall be non-irritating and shall be non- adhering to skin, sutures or to the surgical site. Both ends of the finished pad shall be rounded. The finished pad shall not ravel, tear or bu

10、nch during use. The finished gad shall have a minimum weight of 24 grams and the pad shall absorb a minimum of 8 times its weight of water. Workmanship. The gad shall be free from defects which detract from its appearance or impair its serviceability. Unit, Package (PG). Fifteen pads shall be packag

11、ed in a bag capable of maintaining cleanliness of the pads, Each pad shall be supplied in a plastic disposal bag, OK, as an alternate, 15 plastic disposal bags shall be included with the pads. One package containing 12 bags of 15 pads each (180 pads), as specified, constitutes one unit. Quality Assu

12、rance Provisions. Responsibility for inspection. Unless otherwise spec fied 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 contract or purchase order, the contractol: may us

13、e 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 sup

14、plies and services conform to prescribed requirements. Records. Records of examinations and test performed by or for the contractor shall be maintained by the contractor and made available to the Government upon the Governments request, at any time, or from time to time, during the performance of th

15、e contract and for a period of three years after delivery of the supplies to which such records relate, 2 Provided by IHSNot for ResaleNo reproduction or networking permitted without license from IHS-,-,-A-A-54173 b5 W 9979974 005b7bl O W A-A-5 4 19 3 Inspection. Inspection, as used herein, is defin

16、ed 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. Testing and examination shall be conducted to determine compliance with all

17、 specification requirements. Test methods shall be suitable, accurate and reproducible. Sampling for examination. Sampling for examination shall be conducted in accordance with MIL-STD-105 and as specified herein. The unit of product for examination shall be one bad. otherwise specified, sampling fo

18、r examination shall be conducted at inspection level II, AQL 2.5 maximum percent defective. Unless 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, standar

19、ds, 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. Metric products. Products manufactured to metric dimensions will be considered on

20、an equal basis with those manufactured using inch-pound units, providing they fall within the tolerances specified using conversion tablets contained in the latest revision of Federal Standard No. 376, and all other requirements of this document are met. If a product is manufactured to metric dimens

21、ions and those dimensions exceed the tolerances specified in the inch/pound units, a request should be made to the contracting officer to determine if the product is acceptable. The contracting officer has the option of accepting or rejecting the product. 3 Provided by IHSNot for ResaleNo reproducti

22、on or networking permitted without license from IHS-,-,-A-A-54173 65 7799974 0056762 2 A-A-54 19 3 Regulatory requirements. Federal Food, Drug and Cosmetic Act. by this document has been determined by the U.S. Food and Drug Administration to be under its jurisdiction, the offeror/contractor shall co

23、mply, and be responsible for compliance by its subcontractors/suppliers, with the requirements of the Federal Food, Drug and Cosmetic Actp as amended, and regulations promulgated thereunder. In addition, the offeror/contractor shall comply, and be responsible for compliance by its subcon%ractQrs/sup

24、pliers, with the requirements of all other applicable Federal, State, and local statutes, ordinances, and regulations, use recovered material in accordance with Federal Acquisition Regulation Subpart 23.4 to the maximum extent practical. Preservation, packaging, packing, labeling, and marking. Unles

25、s otherwise specified, preservation, packaging, and packing shal1 be to a degree of protection to preclude damage to containers and/or contents thereo under normal shipping conditions, handling, etc., involving shipment from the supply source to the receiving activity, plus reshipment from receiving

26、 activity, and shall conform to applicable carriers rules and regulations. Intermediate and exterior package quantities and labeling and marking shall be as specified in the contract and/or order. If the product covered t Recovered materials. The offeror/contractor is encouraged to NOTE: document: T

27、he following National Stock Numbei: is covered by this NSN ITEM I BENT IF I CAT I ON - 6510-01-293-5596 PAD, POST-SURGICAL-OBSTRETRICAL, BELTLESS, POSTPARTUM OR POSTOPERATIVE, 180s Ordering data, Inspec%ion/%est dating required, inkerrnediate/exterior package quantities and labeling and marking must

28、 be specified in the contract and/or order. 4 Provided by IHSNot for ResaleNo reproduction or networking permitted without license from IHS-,-,-I l l l I l l l I i l l l l I I I I I I I I I I I I I I I I I I I I l l I l I l 1 A-A-54173 65 W 7777774 0056763 4 W MILITARY INTERESTS: Custodians: Army - MD Navy - MS Air Force - 03 A-A-5 4 1 9 3 PREPARING ACTIVITY: DoD - MB Agent: DLA-DM CIVIL AGENCY COORDINATING ACTIVITY: VA-OSS PHS FDA-MPQAS PGC 71156 Project No. 6510-0769 5 Provided by IHSNot for ResaleNo reproduction or networking permitted without license from IHS-,-,-