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Acofar

EUDAMED

Class I (EU MDR)

Ref RCC532503

by Eurosirel Spa

Identity

Trade Name
ACOFAR EUDAMED
Device Name
CLOTH ROLL EUDAMED
Model / Reference
RCC532503 EUDAMED

Identifiers

Primary DI / UDI-DI
08470001532503 EUDAMED
Basic UDI-DI
8017990RCYJA EUDAMED
EMDN Code
M050101 PLASTERS ON SPOOLS (ROLLS) EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain 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

Acofar by Eurosirel Spa — 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
Eurosirel Spa
EUDAMED SRN
IT-MF-000005982

Sources (1)

  • EUDAMED 2f211c04-aa1f-4123-a8b6-ec19fb00c649 61 fields · synced Jun 19, 2026