A-A-30099D
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 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 ordinances, statutes, 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 a 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 receiving activity, and shall conform to applicable carrier’s rules and regulations. Intermediate and exterior packaging quantities and labeling and marking shall be as specified in the contract and/or order.
NOTE. The following National Stock Number is covered by this document:
NSN |
ITEM IDENTIFICATION |
TYPE |
6515-00-519-3353 |
Catheterization Kit, Urethral |
I |
6515-00-117-9756 |
Catheterization Kit, Urethral Disposable, with 30 cc Syringe, |
II |
6515-00-334-3477 |
Catheterization Kit, Urethral, w/10 ml Syringe, Sterile, Disposable, 20’s |
III |
6515-01-005-5483 |
Catheterization Kit, Urethral, w/15 French, Red, Rubber Catheter |
IV |
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