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Orbital Retractor, Right

EUDAMED

Class I (EU MDR)

Ref M2-2121

by Medartis AG

Identity

Trade Name
Orbital Retractor, Right EUDAMED
Device Name
Retracting & repositioning Instruments EUDAMED
Model / Reference
M2-2121 EUDAMED

Identifiers

Primary DI / UDI-DI
07630894816697 EUDAMED
Basic UDI-DI
76300378009PJ EUDAMED
EMDN Code
L99 SURGICAL INSTRUMENTS, REUSABLE - OTHER 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

Category: Surgical retraction system, reusable

Orbital Retractor, Right by Medartis AG — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retraction system, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Medartis AG
EUDAMED SRN
CH-MF-000022291
Authorised Representative
Medartis GmbH DE-AR-000005810

Sources (1)

  • EUDAMED f3572a4a-f28e-4474-a036-d027f99de5c4 61 fields · synced Jul 31, 2026