← Back to catalogue

Porte Moniteur

EUDAMED

Class I (EU MDR)

Ref PORTE MONITEURModel 351; 3572BP; 351T; 356T; 356; 3582BP; etc..

by Agencinox Sas

Identity

Device Name
PORTE MONITEUR EUDAMED
Model / Reference
351; 3572BP; 351T; 356T; 356; 3582BP; etc.. EUDAMED
PORTE MONITEUR EUDAMED

Identifiers

Primary DI / UDI-DI
03667106000371 EUDAMED
Basic UDI-DI
366710600012PORTMONITYZ 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

Porte Moniteur 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Agencinox Sas
EUDAMED SRN
FR-MF-000027551

Sources (1)

  • EUDAMED 7345a18c-f8f1-4b8b-9bfe-eb2c876c41d7 61 fields · synced Jul 14, 2026