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Perla® Tl Nav. Bone Screw Screwdriver Cannulated

by Spineart SA

Ref NAV-IN 35 41-N

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number1764045086NAVMESCREWDRIT5 Basic UDI-DI 07640221374974UDI-DIDate28 Jun 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  • Withdrawn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
NAVIGATION REUSABLE INSTRUMENTS IIa SCREWDRIVER
Model / Reference
NAV-IN 35 41-N
Primary DI / UDI-DI
07640221374974
Basic UDI-DI
1764045086NAVMESCREWDRIT5
Direct Marketing DI
07640221374974
EMDN Code
Z12011480 Surgical navigation instruments - hardware accessories
Device Class
Class IIa
EU market of registration
France

Manufacturer details

EUDAMED SRN
CH-MF-000015664
Authorised representative
Alpes CN SAS FR-AR-000013241

Other devices from Spineart

See all devices from Spineart →

Properties

  • Sterile
  • Reusable

Other properties (11)

  • 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