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Evacmat

EUDAMED

Class I (EU MDR)

Ref XTEVACMAT

by Moltoplast GmbH

Identity

Trade Name
EVACMAT EUDAMED
Device Name
Evakuierungsmatten EUDAMED
Model / Reference
XTEVACMAT EUDAMED

Identifiers

Primary DI / UDI-DI
90060183300178 EUDAMED
Basic UDI-DI
9006018MOEVACTD EUDAMED
Direct Marketing DI
90060183300178 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

Evacmat 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 fc4bc81f-a7bf-4e27-9971-b91290988ce2 61 fields · synced Jul 13, 2026