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Forceps JFBF272541D

by Joimax, Inc.

Part of a family of 12 devices: see the family page

Ref JFBF272541D

Forceps JFBF272541D is a Class I device made by Joimax, Inc., registered in EUDAMED on 29 Apr 2024 (Basic UDI-DI 42503371FORCSEMHM) and listed in FDA GUDID since 30 Dec 2022 (UDI-DI 04250337116035), active as of 23 Oct 2026.

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

CE MDR

Valid until

No date given

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

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number42503371FORCSEMHM Basic UDI-DI 04250337116035UDI-DIDate29 Apr 2024RegisteredStatusActive
United StatesGUDID listing GUDID Number04250337116035 UDI-DI Date30 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 42503371FORCSEMHM registered 29 Apr 2024 Active
  • FDA GUDID UDI-DI 04250337116035 listed 30 Dec 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04250337116035
  2. Registered EUDAMED 42503371FORCSEMHM

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  • Withdrawn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
Semi-Flexible Biopsy Forceps 30°, down-biting EUDAMED
Forceps GUDID
Generic name
Flexible endoscopic biopsy forceps, reusable
Device name
Semi-Flexible Grasper Forceps
Model / Ref / Catalog
JFBF272541D
Primary DI / UDI-DI
04250337116035
Basic UDI-DI
42503371FORCSEMHM
Direct marketing DI
04250337116035
FDA product code
GEN
EMDN code
L110602 Neurosurgery grippers, reusable
GMDN term
Flexible endoscopic biopsy forceps, reusable
Device class
Class I
Regulation number
878.4800
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Flexible endoscopic biopsy forceps, reusable

Similar devices in this category

Other devices filed under NEUROSURGERY AND SPINAL SURGERY INSTRUMENTS, REUSABLE.

Other devices from Joimax, Inc.

See all devices from Joimax, Inc. →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (19, all answered No)