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Assistant muet

EUDAMED

Class I (EU MDR)

Ref ASSISTANT MUET

by Agencinox Sas

Identity

Device Name
Assistant muet EUDAMED
Model / Reference
ASSISTANT MUET EUDAMED

Identifiers

Primary DI / UDI-DI
03667106000227 EUDAMED
Basic UDI-DI
3667106AssistantmuetJX 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

Assistant muet by Agencinox Sas — 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
Agencinox Sas
EUDAMED SRN
FR-MF-000027551

Sources (1)

  • EUDAMED e67f5699-8e75-47ba-987a-7e7dfe40c1ce 61 fields · synced Oct 6, 2026