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21 CFR 660.30

§ 660.30 Reagent Red Blood Cells.

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

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21 CFR 660.30, § 660.30 Reagent Red Blood Cells, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/88552
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(a) Proper name and definition. The proper name of the product shall be Reagent Red Blood Cells, which shall consist of a preparation of human red blood cells used to detect or identify human blood-group antibodies. (b) Source. Reagent Red Blood Cells shall be prepared from human peripheral blood meeting the criteria of §§ 660.31 and 660.32 of this chapter, or from umbilical cord cells which shall be collected and prepared according to the manufacturer's biologics license application.

Legislative history

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