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Operion 322 (aiims)

EUDAMED

Class I (EU MDR)

Ref OP-322BRT1-AIIMSModel Wall System Monitor

by Rein medical GmbH

Identity

Trade Name
OPERION 322 (AIIMS) EUDAMED
Device Name
WS22AIO.1 EUDAMED
Model / Reference
Wall System Monitor EUDAMED
OP-322BRT1-AIIMS EUDAMED

Identifiers

Primary DI / UDI-DI
04061631010710 EUDAMED
Basic UDI-DI
406163100000WS22AIO1YN EUDAMED
Direct Marketing DI
04061631010710 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I 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

Operion 322 (aiims) by Rein medical 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
Rein medical GmbH
EUDAMED SRN
DE-MF-000018721

Sources (1)

  • EUDAMED c4db2b5b-e160-46ab-9c28-b6db6e86daec 61 fields · synced Jun 19, 2026