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Polypectomy Snare (NON-ELECTRICAL) MD-E-FL181518

by Zhejiang Chuangxiang Medical Technology 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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06936534328942 UDI-DI Date29 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  • Withdrawn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
Polypectomy Snare (NON-ELECTRICAL)
Generic Name
Mechanical-cutting endoscopic polypectomy snare
Model / Reference
MD-E-FL181518
Primary DI / UDI-DI
06936534328942
FDA Product Code
FGX
GMDN Term
Mechanical-cutting endoscopic polypectomy snare
Device Class
Class I
Regulation Number
876.4730
GUDID distribution status
In Commercial Distribution

Other devices from Zhejiang Chuangxiang Medical Technology Co., LTD.

See all devices from Zhejiang Chuangxiang Medical Technology Co., LTD. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No