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Alpha Trancell

EUDAMED

Class IIa (EU MDR)

Ref ALT04ESModel 648305BG

by ArjoHuntleigh AB

Identity

Trade Name
Alpha Trancell EUDAMED
Device Name
ALPHA ACTIVE 3 PUMP EUDAMED
Model / Reference
648305BG EUDAMED
ALT04ES EUDAMED

Identifiers

Primary DI / UDI-DI
05055982788809 EUDAMED
Basic UDI-DI
5060693520020VD EUDAMED
EMDN Code
Z12019003 WOUND TREATMENT EQUIPMENT EUDAMED

Classification

Device Class
Class IIa 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

Alpha Trancell by Arjohuntleigh AB — Class IIa — 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
ArjoHuntleigh AB
EUDAMED SRN
SE-MF-000000696

Sources (1)

  • EUDAMED f275f067-d5f8-47f5-b538-93a9c8802e22 61 fields · synced Jun 18, 2026