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Maxi Move

EUDAMED

Class I (EU MDR)

Ref KMCSAE-C-11Model KHA1010

by ArjoHuntleigh AB

Identity

Trade Name
Maxi Move EUDAMED
Device Name
Tenor EUDAMED
Model / Reference
KHA1010 EUDAMED
KMCSAE-C-11 EUDAMED

Identifiers

Primary DI / UDI-DI
05055982765602 EUDAMED
Basic UDI-DI
5060693520082W3 EUDAMED
EMDN Code
V0805030102 ELECTRIC MOBILE LIFTS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Sweden 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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Maxi Move 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 10939488-54d2-4150-a122-3c4875af081a 61 fields · synced May 22, 2026