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Newmedi

EUDAMED

Class I (EU MDR)

Ref AIM390

by Newmedi

Identity

Trade Name
Newmedi EUDAMED
Device Name
Support K7/Capteur à ventouses EUDAMED
Model / Reference
AIM390 EUDAMED

Identifiers

Primary DI / UDI-DI
37603019409136 EUDAMED
Basic UDI-DI
3760301940913W6 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

Newmedi 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 567a5d52-b7aa-4025-9c90-52c60d39c68c 61 fields · synced Jun 19, 2026