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Maxi Sky 1000

EUDAMED

Class I (EU MDR)

Ref LF21000-EUUKModel MS010-02-03

by ArjoHuntleigh AB

Identity

Trade Name
Maxi Sky 1000 EUDAMED
Device Name
Maxi Sky 2 EUDAMED
Model / Reference
MS010-02-03 EUDAMED
LF21000-EUUK EUDAMED

Identifiers

Primary DI / UDI-DI
05055982770576 EUDAMED
Basic UDI-DI
5060693520105VN EUDAMED
EMDN Code
Z12069001 ELECTRIC HOISTS AND WALKERS 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

Maxi Sky 1000 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 a60f5f26-4ce2-4dec-a87b-a310d7703907 61 fields · synced May 22, 2026