← Back to catalogue

4-motion® Trochleafeile

EUDAMED

Class I (EU MDR)

Ref 9211410

by ARTIQO GmbH

Identity

Trade Name
4-motion® Trochleafeile EUDAMED
Device Name
Klasse Ir Instrumente, allgemeine chirurgisch invasive des 4-motion® Kniesystems, wiederverwendbar; sonstige wiederverwendbare invasive Instrumente EUDAMED
Model / Reference
9211410 EUDAMED

Identifiers

Primary DI / UDI-DI
04251143403715 EUDAMED
Basic UDI-DI
42511434012001BS EUDAMED
Direct Marketing DI
04251143403715 EUDAMED
EMDN Code
L091202 ORTHOPAEDIC SURGERY FILES, REUSABLE EUDAMED

Classification

Device Class
Class I 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

4-motion® Trochleafeile by ARTIQO GmbH — Class I — 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 61743aa0-5df4-4327-b9bb-db3fb4a02330 61 fields · synced Jun 18, 2026