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Punch

by Joimax GmbH 8 variants

Part of a family of 18 devices: see the family page

Ref THP243555

Punch (THP243555) is a Class I device made by Joimax GmbH, registered in EUDAMED on 29 Apr 2024 (Basic UDI-DI 42503371FORCPUNJQ) and listed in FDA GUDID since 27 Oct 2026 (UDI-DI 04250337121947), active as of 9 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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing GUDID Number04250337121947 UDI-DI Date27 Oct 2026ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED Number42503371FORCPUNJQ Basic UDI-DI 04250337121947UDI-DIDate29 Apr 2024RegisteredStatusActive

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 42503371FORCPUNJQ registered 29 Apr 2024 Active
  • FDA GUDID UDI-DI 04250337121947 listed 27 Oct 2026 Listed

Timeline

2 dated events

  1. Registered EUDAMED 42503371FORCPUNJQ
  2. Listed FDA GUDID 04250337121947

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  • Withdrawn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

Generic name
Rigid endoscopic biopsy forceps, reusable
Device name
Eagle Hook Punch
Model / reference
THP243555
Primary DI / UDI-DI
04250337121947
Basic UDI-DI
42503371FORCPUNJQ
Direct marketing DI
04250337121947
FDA product code
LRY
EMDN code
L110602 Neurosurgery grippers, reusable
GMDN term
Rigid 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

Manufacturer details

EUDAMED SRN
DE-MF-000009201

Similar devices in this category

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

Other devices from Joimax GmbH

See all devices from Joimax GmbH →

Properties

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