Skip to content

Guide

by FX Shoulder Solutions 2 variants

Part of a family of 34 devices: see the family page

Ref 941-0120

Guide (941-0120) is a Class I device made by FX Shoulder Solutions, registered in EUDAMED on 22 Jun 2026 (Basic UDI-DI 37010373GUIDECV), active as of 22 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number37010373GUIDECV Basic UDI-DI 03701037320419UDI-DIDate22 Jun 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Guide
Model / reference
941-0120
Primary DI / UDI-DI
03701037320419
Basic UDI-DI
37010373GUIDECV
Direct marketing DI
03701037320419
EMDN code
L091199 Orthopaedic prosthetics instruments, reusable - other
Device class
Class I
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000000465

Similar devices in this category

Other devices filed under ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER.

Other devices from FX Shoulder Solutions

See all devices from FX Shoulder Solutions →

Properties

  • Sterilise before use
  • Reusable
Other properties (12, all answered No)