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Momat®

EUDAMED

Class I (EU MDR)

Ref XMOMAT123AFNÖ

by Moltoplast GmbH

Identity

Trade Name
MOMAT® EUDAMED
Device Name
Sturzmatten ohne Alarmfunktion EUDAMED
Model / Reference
XMOMAT123AFNÖ EUDAMED

Identifiers

Primary DI / UDI-DI
90060183200560 EUDAMED
Basic UDI-DI
9006018MOMASTUL EUDAMED
Direct Marketing DI
90060183200560 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® 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 a72bbdf3-65d7-4e93-9af8-c48ca30e27c9 61 fields · synced Jun 19, 2026