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GD - Device Carriers

EUDAMED

Class I (EU MDR)

Ref GD60SX0008-DRModel GD

by MAVIG GmbH

Identity

Device Name
GD - Device Carriers EUDAMED
Model / Reference
GD EUDAMED
GD60SX0008-DR EUDAMED

Identifiers

Primary DI / UDI-DI
04251339906372 EUDAMED
Basic UDI-DI
4251339906310WF EUDAMED
Direct Marketing DI
04251339906372 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

GD - Device Carriers by MAVIG GmbH — 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
MAVIG GmbH
EUDAMED SRN
DE-MF-000006207

Sources (1)

  • EUDAMED d11bef52-64d0-45f9-8ac8-fabfe1617b9e 61 fields · synced Jul 13, 2026