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AluBurn

EUDAMED

Class I (EU MDR)

Ref ALUBPAD5050

by Pharmaplast

Identity

Trade Name
AluBurn EUDAMED
Device Name
Non-adherent wound pad EUDAMED
Model / Reference
ALUBPAD5050 EUDAMED

Identifiers

Primary DI / UDI-DI
06222023835153 EUDAMED
Basic UDI-DI
62220238PharmaPadZF EUDAMED
EMDN Code
M040204 NON-ADHERENT ABSORBENT DRESSINGS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Portugal EUDAMED

Clinical & Handling

Sterile

Yes

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

AluBurn 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 0fc134f7-d60a-4134-b345-38cee5da786a 61 fields · synced Sep 18, 2026