Skip to content

Registration Probe

by Claronav Kolahi

Ref 950-NS-RP

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number7540209955-NC-RSI46 Basic UDI-DI 07540209956072UDI-DIDate31 Aug 2026RegisteredStatusActive

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  • Withdrawn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
Navient reusable surgical instruments
Model / Reference
950-NS-RP
Primary DI / UDI-DI
07540209956072
Basic UDI-DI
7540209955-NC-RSI46
Direct Marketing DI
07540209956072
EMDN Code
Z12011480 Surgical navigation instruments - hardware accessories
Device Class
Class I
Market of Registration
France

Manufacturer details

EUDAMED SRN
CA-MF-000037841
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Other devices from Claronav Kolahi

See all devices from Claronav Kolahi →

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