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Versius Bipolar Maryland Grasper

by CMR Surgical Limited EUDAMED

Active European Union

Ref 10200

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number506054821VersiusESN4 Basic UDI-DIDate18 Aug 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

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.

Specification

EUDAMED

Device Name
Versius Electrosurgical Instruments
Model / Reference
10200
Primary DI / UDI-DI
05060548210106
Basic UDI-DI
506054821VersiusESN4
Direct Marketing DI
05060548210106
EMDN Code
L1304 Robotic surgery forceps and graspers, reusable
Device Class
Class IIb
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
GB-MF-000010885
Authorised representative
Advena Limited MT-AR-000000234

Other devices from Cmr Surgical Limited

See all devices from Cmr Surgical Limited →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: 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