Skip to content

Punch, straight

by Joimax GmbH 2 variants

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

Ref THP243545

Punch, straight (THP243545) 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 30 Dec 2022 (UDI-DI 04250337116998), active as of 22 Oct 2026.

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

CE MDR CE MDD

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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED Number42503371FORCPUNJQ Basic UDI-DI 04250337116998UDI-DIDate29 Apr 2024RegisteredStatusActive
European UnionCE/MDR EUDAMED Number42503371FORCPUNJQ Basic UDI-DI 04250337116998UDI-DIDate29 Apr 2024RegisteredStatusActive
United StatesGUDID listing GUDID Number04250337116998 UDI-DI Date30 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 42503371FORCPUNJQ registered 29 Apr 2024 Active· +1 more in the status table
  • FDA GUDID UDI-DI 04250337116998 listed 30 Dec 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04250337116998
  2. Registered EUDAMED 42503371FORCPUNJQ

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
Punch, straight EUDAMED
Forceps GUDID
Generic name
Flexible endoscopic biopsy forceps, reusable
Device name
Eagle Hook Punch
Model / Ref / Catalog
THP243545
Primary DI / UDI-DI
04250337116998
Basic UDI-DI
42503371FORCPUNJQ, B-04250337116998
FDA product code
LRY
EMDN code
L110699 Neurosurgery forceps, reusable - other
GMDN term
Flexible endoscopic biopsy forceps, reusable
Device class
Class I
Regulation number
878.4800
EU registration type
Standard device
Legacy device (under a directive)
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)