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Electronic Code of Federal Regulations

e-CFR data is current as of June 4, 2020

Title 21Chapter ISubchapter HPart 801Subpart B → §801.20


Title 21: Food and Drugs
PART 801—LABELING
Subpart B—Labeling Requirements for Unique Device Identification


§801.20   Label to bear a unique device identifier.

(a) In general. (1) The label of every medical device shall bear a unique device identifier (UDI) that meets the requirements of this subpart and part 830 of this chapter.

(2) Every device package shall bear a UDI that meets the requirements of this subpart and part 830 of this chapter.

(b) Exceptions. Exceptions to the general rule of paragraph (a) of this section are provided by §§801.30, 801.45, and 801.128(f)(2), and §801.55 provides a means to request an exception or alternative not provided by those provisions.

[78 FR 58818, Sept. 24, 2013]

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