Skip to content

QMedix™ DACD113030-1-19

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 Number10850082766007 UDI-DI Date24 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  • Withdrawn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
QMedix™
Generic Name
Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical
Model / Ref / Catalog
DACD113030-1-19, 113030-1-19
Primary DI / UDI-DI
10850082766007
FDA Product Code
JHI
GMDN Term
Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical
Device Class
Class II
Regulation Number
862.1155
GUDID distribution status
In Commercial Distribution

Other devices from Diagnostic Automation, Inc.

See all devices from Diagnostic Automation, Inc. →

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