Skip to content

VisiMARKER

by Clear Guide Medical

Ref CG-VMModel VisiMARKER

VisiMARKER (CG-VM) is a Class I device made by Clear Guide Medical, registered in EUDAMED on 27 May 2026 (Basic UDI-DI B-++B201CGVM0), active as of 24 Oct 2026.

Active European Union

CE MDD

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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-++B201CGVM0 Basic UDI-DI ++B201CGVM0UDI-DIDate27 May 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Clear Guide VisiMARKER
Model / reference
VisiMARKER, CG-VM
Primary DI / UDI-DI
++B201CGVM0
Basic UDI-DI
B-++B201CGVM0
EMDN code
Z12011485 Surgical navigation instruments - consumables
Device class
Class I
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
US-MF-000031413
Authorised representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Similar devices in this category

Other devices filed under SURGICAL NAVIGATION INSTRUMENTS - CONSUMABLES.

Other devices from Clear Guide Medical

See all devices from Clear Guide Medical →

Properties

  • Supplied sterile
Other properties (11, all answered No)