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Parafricta

EUDAMED

Class I (EU MDR)

Ref PFFUG-003XS

by APA Parafricta Ltd

Identity

Trade Name
Parafricta EUDAMED
Device Name
Low Friction Fabric Device EUDAMED
Model / Reference
PFFUG-003XS EUDAMED

Identifiers

Primary DI / UDI-DI
05060162890340 EUDAMED
Basic UDI-DI
506016289PARAFRICTALFFD3R EUDAMED
Direct Marketing DI
05060162890340 EUDAMED
EMDN Code
V0880 MEDICAL SUPPORT EQUIPMENT - ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Belgium 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

Parafricta by APA Parafricta Ltd — 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
APA Parafricta Ltd
EUDAMED SRN
GB-MF-000006298
Authorised Representative
European Healthcare & Device Solutions Ltd. IE-AR-000003999

Sources (1)

  • EUDAMED cc3e108c-2894-4c8b-affc-096c1ff67d5b 61 fields · synced Jun 19, 2026