← Back to catalogue

A2® Schaftraspel 0 G

EUDAMED

Class IIa (EU MDR)

Ref 9110200

by ARTIQO GmbH

Identity

Trade Name
A2® Schaftraspel 0 G EUDAMED
Device Name
Klasse IIa Instrumente, chirurgisch invasiv, wiederverwendbar; schneidende, maschinell angetriebene Instrumente, A2® Schaftraspeln EUDAMED
Model / Reference
9110200 EUDAMED

Identifiers

Primary DI / UDI-DI
04251143402237 EUDAMED
Basic UDI-DI
42511434021001BW EUDAMED
Direct Marketing DI
04251143402237 EUDAMED
EMDN Code
L091201 ORTHOPAEDIC SURGERY RASPS, REUSABLE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

A2® Schaftraspel 0 G by ARTIQO GmbH — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
ARTIQO GmbH
EUDAMED SRN
DE-MF-000007336

Sources (1)

  • EUDAMED 4a13aba6-7192-4157-9e44-7048bc5e9c25 61 fields · synced Jul 17, 2026