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Verso® Glenoid 3.5mm Drill Guide

by Innovative Design Orthopaedics Limited

Ref 402871Model Verso Instruments Set

Active European Union

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number506040645IDO4028VY Basic UDI-DI 05060406450392UDI-DIDate16 Aug 2022RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Verso Instruments Set
Model / Reference
Verso Instruments Set, 402871
Primary DI / UDI-DI
05060406450392
Basic UDI-DI
506040645IDO4028VY
Direct Marketing DI
05060406450392
EMDN Code
L0922 Orthopaedic surgery guides, reusable
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
GB-MF-000026411
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

Other devices from Innovative Design Orthopaedics Limited

Properties

  • Reusable

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No