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Feinnadel zur Schmerztherapie

by Radimed Gesellschaft für Kommunikationsdienstleistungen und Medizintechnik mbH EUDAMED 17 variants

Active European Union

Ref 10012

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number426014668KANUELE018E Basic UDI-DIDate1 Jun 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  • Withdrawn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
Feinnadeln / IMS
Model / Reference
10012
Primary DI / UDI-DI
04260146680603
Basic UDI-DI
426014668KANUELE018E
EMDN Code
A019099 Needles for other procedures - other
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000006540

From the manufacturer

Manufacturer's product page: Thermoläsionskanülen zur Schmerztherapie

Other devices from Radimed Gesellschaft für Kommunikationsdienstleistungen und Medizintechnik mbH

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Properties

  • Sterile

Other properties (12)

  • 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