A-A-30172
Regulatory requirements.
Federal Food, Drug 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 the Federal Food, Drug and Cosmetic Act, as amended, and regulations promulgated thereafter. 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.
Recovered materials. The offeror/contractor is encouraged to use recovered material in accordance with
Federal Acquisition Regulation Subpart 23.4 to the maximum extent practical.
Preservation, packaging, packing, labeling, and marking. Unless otherwise specified, preservation, packaging, and packing shall be to the degree of protection to preclude damage 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 the receiving activity, and shall conform to applicable carrier's rules and regulations. Intermediate and exterior package quantities and labeling and marking shall be that usually provided by the supplier as commercial practice, and as specified in the contract and/or order.
NOTE: The following National Stock Numbers are covered by this document.
NSN |
ITEM DESCRIPTION |
SIZE |
PLY |
UNIT PACKAGE QUANTITY FOR DOD |
6510-00-058-4421 |
SPONGE, SURGICAL 2“ X 2” (5.08 cm x 5.08 cm) |
1 |
8 |
A |
6510-00-559-3219 |
SPONGE, SURGICAL 4” X 4” (10.2 cm x 10.2 cm) |
2 |
12 |
|
6510-00-116-1311 |
SPONGE, SURGICAL 4” X 4” (10.2 cm x 10.2 cm) |
2 |
12 |
B or C |
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