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QuikTox ULTRA DIP 1

by Advin Biotech 4 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 NumberB115QTCARDD12021 UDI-DI Date23 Sep 2026ListedStatusListed 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  • Withdrawn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
QuikTox ULTRA DIP
Generic Name
Multiple drugs of abuse IVD, kit, rapid ICT, clinical
Model / Reference
1
Primary DI / UDI-DI
B115QTCARDD12021
FDA Product Code
DKZ, DIS, JXM, DJG, DIO, NGG, DJC, DJR, LCM, LDJ
GMDN Term
Multiple drugs of abuse IVD, kit, rapid ICT, clinical
Device Class
Class II
Regulation Number
862.3100, 862.3150, 862.3170, 862.3650, 862.3250, 862.3610, 862.3620, 862.3870
GUDID distribution status
In Commercial Distribution

Other devices from Advin Biotech

See all devices from Advin Biotech →

Properties

  • Lot / Batch Number
  • Expiration Date

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No