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Potter Mobile Universel

EUDAMED

Class I (EU MDR)

Ref EIM324

by Newmedi

Identity

Device Name
Potter Mobile Universel EUDAMED
Model / Reference
EIM324 EUDAMED

Identifiers

Primary DI / UDI-DI
37603019403196 EUDAMED
Basic UDI-DI
3760301940318J EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France 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

Potter Mobile Universel by Newmedi — 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
Newmedi
EUDAMED SRN
FR-MF-000000922

Sources (1)

  • EUDAMED cc885c9a-f0e5-4795-8326-473ca17dedd0 61 fields · synced Jun 19, 2026