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4-motion® Probeinlay C h=8

EUDAMED

Class IIa (EU MDR)

Ref 9211308

by ARTIQO GmbH

Identity

Trade Name
4-motion® Probeinlay C h=8 EUDAMED
Device Name
Klasse IIa Instrumente, chirurgisch invasiv, wiederverwendbar; Probeimplantate EUDAMED
Model / Reference
9211308 EUDAMED

Identifiers

Primary DI / UDI-DI
04251143403647 EUDAMED
Basic UDI-DI
42511434022002C7 EUDAMED
Direct Marketing DI
04251143403647 EUDAMED
EMDN Code
L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER 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

4-motion® Probeinlay C h=8 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

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Manufacturer

Manufacturer
ARTIQO GmbH
EUDAMED SRN
DE-MF-000007336

Sources (1)

  • EUDAMED 879c0688-4b8e-4ee4-8d4e-efc48d4e424d 61 fields · synced Sep 17, 2026