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21 C.F.R. Part 830 – Unique Device Identification | Midpage
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Code of Federal Regulations
Title 21
Chapter I
Subchapter H
Part 830
21 C.F.R. Part 830
Unique Device Identification
A
General Provisions
B
Requirements for a Unique Device Identifier
C
FDA Accreditation of an Issuing Agency
D
FDA as an Issuing Agency
E
Global Unique Device Identification Database