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Lame De Gouge À Usage Unique Stériles

by Capron Podologie EUDAMED

Active European Union

Ref 13002Model Réf : 13002-001 n°1, n°2, n°3, n°5, n°8, n°10, n°12

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-37014885BA13002T8W5 Basic UDI-DIDate11 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

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

Model / Reference
Réf : 13002-001 n°1, n°2, n°3, n°5, n°8, n°10, n°12, 13002
Primary DI / UDI-DI
D-37014885BA13002T8W5
Basic UDI-DI
B-37014885BA13002T8W5
EMDN Code
V010302 Blades without safety systems, single-use - not included in other classes
Device Class
Class IIa
Market of Registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000000322

Related devices

Category: Manual scalpel blade, single-use

Other devices from Capron Podologie

See all devices from Capron Podologie →

Properties

  • Sterile

Other properties (10)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No