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AZMED Beige M

by Hengshui Tianjian Medical Supplies 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 Number06973712280456 UDI-DI Date9 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  • Withdrawn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
Azmed
Generic Name
Abdominal binder, reusable
Model / Reference
Beige M
Primary DI / UDI-DI
06973712280456
FDA Product Code
ISR
GMDN Term
Abdominal binder, reusable
Device Class
Class I
Regulation Number
890.3025
GUDID distribution status
In Commercial Distribution

Other devices from Hengshui Tianjian Medical Supplies CO., LTD

See all devices from Hengshui Tianjian Medical Supplies 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