REGULATIONS
Rulings
AD/CVD
Notices
HTSUS
U.S. Code
Regs
More
Ports
About
Updates
Apps
Larger font
Smaller font
CustomsMobile Pro
beta now open!
Apply for a FREE beta account. Spaces are limited so apply today.
SIGNUP FOR BETA
SEARCH
Sort by Rank
Titles Ascending
Titles Descending
10 per page
25 Result/page
50 Result/page
Regulations last checked for updates: Nov 21, 2024
Title 21 - Food and Drugs last revised: Nov 19, 2024
All Titles
Title 21
Chapter I
Part 830 - PART 830—UNIQUE DEVICE IDENTIFICATION
Subpart A [§ 830.3 - § 830.3] - Subpart A—General Provisions
Subpart B [§ 830.10 - § 830.60] - Subpart B—Requirements for a Unique Device Identifier
Subpart C [§ 830.100 - § 830.130] - Subpart C—FDA Accreditation of an Issuing Agency
Subpart D [§ 830.200 - § 830.220] - Subpart D—FDA as an Issuing Agency
Subpart E [§ 830.300 - § 830.360] - Subpart E—Global Unique Device Identification Database
authority:
21 U.S.C. 321
,
331
,
352
,
353
,
360
,
360
d,
360
i,
360
j,
371
source:
78 FR 58823, Sept. 24, 2013, unless otherwise noted.
.list_box li,p,.cm-search-info,.cm-search-detail,.abt span,.expand-collapse_top
Get the CustomsMobile app!