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21 CFR 640.50

§ 640.50 Cryoprecipitated AHF.

United States · 21 CFR — Food and Drugs · Status: effective

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21 CFR 640.50, § 640.50 Cryoprecipitated AHF, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/88491
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(a) Proper name and definition. The proper name of this product shall be Cryoprecipitated AHF. The product is defined as a preparation of antihemophilic factor, which is obtained from a single unit of plasma collected and processed in a closed system. (b) Source. The source material for Cryoprecipitated AHF shall be plasma which may be obtained by whole blood collection or by plasmapheresis.

Legislative history

This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.