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Single Use Biopsy Forceps MD-A-BF2403

by Zhejiang Chuangxiang Medical Technology Co., LTD. 2 variants

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing GUDID Number06970401816927 UDI-DI Date30 Dec 2022ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED Number— Date—StatusActive

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Single Use Biopsy Forceps
Generic Name
Flexible endoscopic biopsy forceps, single-use
Model / Reference
MD-A-BF2403
Primary DI / UDI-DI
06970401816927
FDA Product Code
FCL
GMDN Term
Flexible endoscopic biopsy forceps, single-use
Device Class
Class I
Regulation Number
876.1075
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

Other properties (8)

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