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Localizer Adhesive Pad - Single use

by Fiagon GmbH EUDAMED

Active European Union

Ref E 01 3202Model Patient reference device for navigation

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number426075993E0066K Basic UDI-DIDate21 Nov 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

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

Specification

EUDAMED

Model / Reference
Patient reference device for navigation, E 01 3202
Primary DI / UDI-DI
04260759931628
Basic UDI-DI
426075993E0066K
Direct Marketing DI
04260759931628
EMDN Code
Z12011480 Surgical navigation instruments - hardware accessories
Device Class
Class I
Market of Registration
Cyprus

Manufacturer details

EUDAMED SRN
DE-MF-000010763

Other devices from Fiagon GmbH

See all devices from Fiagon GmbH →

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