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Afre

EUDAMED

Class I (EU MDR)

Ref DM1040305B

by Abílio Freire Lda

Identity

Trade Name
AFRE EUDAMED
Device Name
Ligaduras Ortopédicas EUDAMED
Model / Reference
DM1040305B EUDAMED

Identifiers

Primary DI / UDI-DI
05600710211335 EUDAMED
Basic UDI-DI
5600710211DM104E2 EUDAMED
Direct Marketing DI
05600710211335 EUDAMED
EMDN Code
M03050299 BANDAGES AND SPLINTS - OTHER 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

Category: Hand/finger splint, reusable

Afre by Abílio Freire Lda — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Hand/finger splint, reusable.

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 2cbb843a-c153-482b-bb6a-7ccd3e569fb4 61 fields · synced Sep 17, 2026