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Bohrführung für RM-System inkl. Schraubhilfe für Medtronic Visualase

by inomed Medizintechnik GmbH

Ref 590320

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, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number42503076FZS220AZ Basic UDI-DI 04250307609802UDI-DIDate12 May 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
590320
Primary DI / UDI-DI
04250307609802
Basic UDI-DI
42503076FZS220AZ
EMDN Code
Z12100680 Stereotactic neurosurgery instruments - hardware accessories
Device Class
Class I
Medical Purpose
Indicated for the use during stereotactic interventions

Manufacturer details

EUDAMED SRN
DE-PR-000019534

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Properties

Other properties (1)

  • Sterile: No