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Momat® Alarm

EUDAMED

Class I (EU MDR)

Ref 6501010000

by Moltoplast GmbH

Identity

Trade Name
MOMAT® ALARM EUDAMED
Device Name
Sturzmatten mit Alarmfunktion EUDAMED
Model / Reference
6501010000 EUDAMED

Identifiers

Primary DI / UDI-DI
90060183100198 EUDAMED
Basic UDI-DI
9006018MOMAALSE EUDAMED
Direct Marketing DI
90060183100198 EUDAMED
EMDN Code
V0899 MEDICAL SUPPORT EQUIPMENT - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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

Momat® Alarm by Moltoplast GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Moltoplast GmbH
EUDAMED SRN
AT-MF-000004503

Sources (1)

  • EUDAMED 62fd3c19-c49e-40cd-8fb8-9d911a47a397 61 fields · synced Jun 19, 2026