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QuikTox Ultra Cup Rapid Drug Test 1

by Advin Biotech 6 variants

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

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 NumberB115VQTCUPD16381 UDI-DI Date23 Sep 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
QuikTox Ultra Cup Rapid Drug Test
Generic Name
Test tube heater
Model / Reference
1
Primary DI / UDI-DI
B115VQTCUPD16381
510(k) Number
FDA Product Code
NFT, PTH, NGL, NFV, NFY, PTG, NGG, NGM, QAW, NFW
GMDN Term
Test tube heater
Device Class
Class II
Regulation Number
862.3100, 862.3150, 862.3650, 862.3170, 862.3250, 862.3620, 862.3610, 862.3910, 862.3870
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K252867)

Show all (12)

Other devices from Advin Biotech

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Properties

  • Single Use
  • Lot / Batch Number
  • Expiration Date

Other properties (11)

  • Sterile: 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