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Instrument Case, MIDFACE

EUDAMED

Class I (EU MDR)

Ref M2-6005.002

by Medartis AG

Identity

Trade Name
Instrument Case, MIDFACE EUDAMED
Device Name
Container EUDAMED
Model / Reference
M2-6005.002 EUDAMED

Identifiers

Primary DI / UDI-DI
07630037855590 EUDAMED
Basic UDI-DI
76300378000NY EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

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: Device sterilization/disinfection container, reusable

Instrument Case, MIDFACE by Medartis AG — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, 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 84890c9c-1b55-4ff5-ab6f-13bfc82b5058 61 fields · synced Jul 23, 2026