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Cure-Aid® Dermi plaster

EUDAMED

Class I (EU MDR)

Ref DERMIN80100

by Pharmaplast

Identity

Trade Name
Cure-Aid® Dermi plaster EUDAMED
Device Name
Cure Aid Non-Sterile Product line EUDAMED
Model / Reference
DERMIN80100 EUDAMED

Identifiers

Primary DI / UDI-DI
06223004867453 EUDAMED
Basic UDI-DI
62220238CureAidNSQ7 EUDAMED
EMDN Code
M030102 NON-WOVEN BANDAGES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Northern Ireland 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

Cure-Aid® Dermi plaster by Pharmaplast — 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
Pharmaplast
EUDAMED SRN
EG-MF-000004501
Authorised Representative
E C REP LIMITED IE-AR-000003995

Sources (1)

  • EUDAMED c8a1cdd8-0d0b-4fb5-b437-090308fe7336 61 fields · synced Jun 18, 2026