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Maxi Sky 2

EUDAMED

Class I (EU MDR)

Ref MS103-01-06Model MS010-02-03

by ArjoHuntleigh AB

Identity

Trade Name
Maxi Sky 2 EUDAMED
Device Name
Maxi Sky 2 EUDAMED
Model / Reference
MS010-02-03 EUDAMED
MS103-01-06 EUDAMED

Identifiers

Primary DI / UDI-DI
05056097328607 EUDAMED
Basic UDI-DI
5060693520105VN EUDAMED
EMDN Code
Z12069001 ELECTRIC HOISTS AND WALKERS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France 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

Maxi Sky 2 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 7b20d267-429d-4759-817a-bbd6c7e9d33b 61 fields · synced May 22, 2026