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QMedix™ DACD121089-1-21

by Diagnostic Automation, Inc.

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 Number00894175000091 UDI-DI Date30 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  • Withdrawn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
QMedix™
Generic Name
Multiple therapeutic drugs/drugs of abuse IVD, kit, thin layer chromatography
Model / Ref / Catalog
DACD121089-1-21, 121089-1-21
Primary DI / UDI-DI
00894175000091
FDA Product Code
DJG, LAF, LCM, LDJ, DIO
GMDN Term
Multiple therapeutic drugs/drugs of abuse IVD, kit, thin layer chromatography
Device Class
Class II
Regulation Number
862.3650, 862.3610, 862.3870, 862.3250
GUDID distribution status
In Commercial Distribution

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Properties

  • Single Use
  • Convenience Kit
  • Lot / Batch Number
  • Expiration Date

Other properties (10)

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