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Maxi Sky 2

EUDAMED

Class I (EU MDR)

Ref MS011-G1-08Model 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
MS011-G1-08 EUDAMED

Identifiers

Primary DI / UDI-DI
05055982772143 EUDAMED
Basic UDI-DI
5060693520105VN EUDAMED
EMDN Code
Z12069001 ELECTRIC HOISTS AND WALKERS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Ireland 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 899bddb8-4efd-4f1c-94dd-8b41e1648e5e 61 fields · synced May 29, 2026