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Afre

EUDAMED

Class I (EU MDR)

Ref DM1031010B

by Abílio Freire Lda

Identity

Trade Name
AFRE EUDAMED
Device Name
Ligaduras de Gaze EUDAMED
Model / Reference
DM1031010B EUDAMED

Identifiers

Primary DI / UDI-DI
05600710211311 EUDAMED
Basic UDI-DI
5600710211DM103DY EUDAMED
Direct Marketing DI
05600710211311 EUDAMED
EMDN Code
M030101 HYDROPHILIC GAUZE BANDAGES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Portugal 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

Afre by Abílio Freire Lda — 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
Abílio Freire Lda
EUDAMED SRN
PT-MF-000022553

Sources (1)

  • EUDAMED 2a70209b-7cc5-4947-9db6-fb76e7dcf853 61 fields · synced Sep 17, 2026