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A2® Schaftraspel 7 G

by ARTIQO GmbH Germany EUDAMED

Ref 9110207 EMDN L091201

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number42511434021001BW Basic UDI-DIDate22 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 25 Oct 2026

Device Name
Klasse IIa Instrumente, chirurgisch invasiv, wiederverwendbar; schneidende, maschinell angetriebene Instrumente, A2® Schaftraspeln
Model / Reference
9110207
Primary DI / UDI-DI
04251143402305
Basic UDI-DI
42511434021001BW
Direct Marketing DI
04251143402305
EMDN Code
L091201 Orthopaedic surgery rasps, reusable
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000007336

Other devices from ARTIQO GmbH

See all devices from ARTIQO GmbH →

Properties & raw data

Show properties, registry sources and raw records
  • 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

Sources (1)

  • EUDAMED 04251143402305|42511434021001BW 61 fields · synced 25 Oct 2026