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ALVO Integra 222

EUDAMED

Class I (EU MDR)

Ref AL-222FBT5.1Model Wall System Monitor

by Rein medical GmbH

Identity

Trade Name
ALVO Integra 222 EUDAMED
Device Name
WS22AIO.1 EUDAMED
Model / Reference
Wall System Monitor EUDAMED
AL-222FBT5.1 EUDAMED

Identifiers

Primary DI / UDI-DI
04061631136045 EUDAMED
Basic UDI-DI
406163100000WS22AIO1YN EUDAMED
Direct Marketing DI
04061631136045 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 222 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 2a43fdd9-9a56-400b-9439-69f06b35670d 61 fields · synced Jun 19, 2026