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Evermed CLF-B106

by Xiamen Taft Medical Co., Ltd.

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06972077026341 UDI-DI Date6 May 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  • Withdrawn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
Evermed
Generic Name
Francisella tularensis antigen IVD, kit, rapid ICT, clinical
Model / Reference
CLF-B106
Primary DI / UDI-DI
06972077026341
FDA Product Code
KNN
GMDN Term
Francisella tularensis antigen IVD, kit, rapid ICT, clinical
Device Class
Class I
Regulation Number
890.3920
GUDID distribution status
In Commercial Distribution

Other devices from Xiamen Taft Medical Co., Ltd.

See all devices from Xiamen Taft Medical Co., Ltd. →

Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Serial Number
  • Manufacturing Date

Other properties (10)

  • 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
  • Expiration Date: No