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ALVO Integra 322

EUDAMED

Class I (EU MDR)

Ref AL-322FBT1.0Model Wall System MonitorRef AL-322FBT3.0

by Rein medical GmbH

Identity

Trade Name
ALVO Integra 322 EUDAMED
Device Name
WS22AIO.1 EUDAMED
WS22AIO.2 EUDAMED
Model / Reference
Wall System Monitor EUDAMED
AL-322FBT1.0 EUDAMED
AL-322FBT3.0 EUDAMED

Identifiers

Primary DI / UDI-DI
04061631136052 EUDAMED
04061631136076 EUDAMED
Basic UDI-DI
406163100000WS22AIO1YN EUDAMED
406163100000WS22AIO2YQ EUDAMED
Direct Marketing DI
04061631136052 EUDAMED
04061631136076 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

ALVO Integra 322 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 (2)

  • EUDAMED da13f139-c4eb-4b81-aafa-db65e72f3fff 61 fields · synced Oct 6, 2026
  • EUDAMED 0f8c1334-b2cb-4e8c-8afd-7e60251ffbfb 61 fields · synced May 17, 2026