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Tweezer JAF180023

by Joimax GmbH

Ref JAF180023

Tweezer JAF180023 is a suturing needle holder (EU MDR Class I; FDA Class I; FDA product code GEN, Forceps, General & Plastic Surgery) made by Joimax GmbH, registered in EUDAMED on 21 May 2026 (Basic UDI-DI 42503371FORCTWEJY) and listed in FDA GUDID since 30 Dec 2022 (UDI-DI 04250337103004), active as of 12 Nov 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number42503371FORCTWEJY Basic UDI-DI 04250337103004UDI-DIDate21 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04250337103004 UDI-DI Date30 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 42503371FORCTWEJY registered 21 May 2026 Active
  • FDA GUDID UDI-DI 04250337103004 listed 30 Dec 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04250337103004
  2. Registered EUDAMED 42503371FORCTWEJY

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  • Withdrawn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
Tweezers EUDAMED
Tweezer GUDID
Generic name
Suturing needle holder, reusable
Model / Ref / Catalog
JAF180023
Primary DI / UDI-DI
04250337103004
Basic UDI-DI
42503371FORCTWEJY
Direct marketing DI
04250337103004
FDA product code
GEN
EMDN code
L031308 Surgical and anatomical tweezers, reusable
GMDN term
Suturing needle holder, 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: Suturing needle holder, reusable

Similar devices in this category

Other devices filed under SURGICAL AND ANATOMICAL TWEEZERS, REUSABLE.

Other devices from Joimax GmbH

See all devices from Joimax GmbH →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (20, all answered No)