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Identify Diagnostics Drug Test Cups ID-CP12-BUP-AZ175

by Medical Distribution Group Inc 2 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10850013035738 UDI-DI Date4 Dec 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Identify Diagnostics Drug Test Cups
Generic Name
Multiple drugs of abuse IVD, kit, rapid ICT, clinical
Model / Ref / Catalog
ID-CP12-BUP-AZ175
Primary DI / UDI-DI
10850013035738
FDA Product Code
DJR, DIS, JXM, LCM, DJC, DKZ, DJG, DIO, LDJ
GMDN Term
Multiple drugs of abuse IVD, kit, rapid ICT, clinical
Device Class
Class II
Regulation Number
862.3620, 862.3150, 862.3170, 862.3610, 862.3100, 862.3650, 862.3250, 862.3870
GUDID distribution status
In Commercial Distribution

Other devices from Medical Distribution Group Inc

See all devices from Medical Distribution Group Inc →

Properties

  • Single Use
  • Prescription Use
  • Over-the-Counter
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No