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Alenti

EUDAMED

Class I (EU MDR)

Ref CDB8101-01

by ArjoHuntleigh AB

Identity

Trade Name
Alenti EUDAMED
Device Name
ALENTI EUDAMED
Model / Reference
CDB8101-01 EUDAMED

Identifiers

Primary DI / UDI-DI
05055982787932 EUDAMED
Basic UDI-DI
5060693520259WJ EUDAMED
EMDN Code
V08050399 PATIENT TRANSFER LIFTS - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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

Alenti by Arjohuntleigh AB — 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
ArjoHuntleigh AB
EUDAMED SRN
SE-MF-000000696

Sources (1)

  • EUDAMED ed00185c-909c-4f09-8700-96e499504554 61 fields · synced Jun 18, 2026