21 C.F.R. · Food and Drugs
21 C.F.R. § 830.120

Responsibilities of an FDA-accredited issuing agency.

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21 C.F.R. § 830.120 — Responsibilities of an FDA-accredited issuing agency.

§ 830.120 Responsibilities of an FDA-accredited issuing agency. To maintain its accreditation, an issuing agency must: (a) Operate a system for assignment of unique device identifiers (UDIs) that meets the requirements of § 830.20; (b) Make available information concerning its system for the assignment of UDIs; (c) Maintain a list of labelers that use its system for the assignment of UDIs and provide FDA a copy of such list in electronic form by December 31 of each year; (d) Upon request, provide FDA with information concerning a labeler that is employing the issuing agency's system for assignment of UDIs; and (e) Remain in compliance with the eligibility and accreditation criteria set forth in § 830.100.

Source: ecfr.gov · govinfo.gov — public domain Official Source ↗
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21 C.F.R. § 830.120
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The regulatory text of 21 C.F.R. § 830.120 is reproduced from the official Code of Federal Regulations as published by the Office of the Federal Register and the National Archives and Records Administration.
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