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counterholder JMPS1045ST

by Joimax GmbH

Ref JMPS1045ST

counterholder JMPS1045ST is a Class I device made by Joimax GmbH, registered in EUDAMED on 21 May 2026 (Basic UDI-DI 42503371INSRHOLML) and listed in FDA GUDID since 30 Dec 2022 (UDI-DI 04250337107903), 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 Number42503371INSRHOLML Basic UDI-DI 04250337107903UDI-DIDate21 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04250337107903 UDI-DI Date30 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 42503371INSRHOLML registered 21 May 2026 Active
  • FDA GUDID UDI-DI 04250337107903 listed 30 Dec 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04250337107903
  2. Registered EUDAMED 42503371INSRHOLML

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  • Withdrawn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
counterholder
Generic name
General internal orthopaedic fixation system implantation kit
Model / Ref / Catalog
JMPS1045ST
Primary DI / UDI-DI
04250337107903
Basic UDI-DI
42503371INSRHOLML
Direct marketing DI
04250337107903
FDA product code
LXH
EMDN code
L1199 Neurosurgery instruments, reusable - other
GMDN term
General internal orthopaedic fixation system implantation kit
Device class
Class I
Regulation number
888.4540
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: General internal orthopaedic fixation system implantation kit

Similar devices in this category

Other devices filed under NEUROSURGERY INSTRUMENTS, REUSABLE - OTHER.

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)