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Maxi Move 5

EUDAMED

Class I (EU MDR)

Ref KMESS0-0Model HEB0000

by ArjoHuntleigh AB

Identity

Trade Name
Maxi Move 5 EUDAMED
Device Name
SARA FLEX EUDAMED
Model / Reference
HEB0000 EUDAMED
KMESS0-0 EUDAMED

Identifiers

Primary DI / UDI-DI
05059441438168 EUDAMED
Basic UDI-DI
5060693520112VK EUDAMED
EMDN Code
V0805030102 ELECTRIC MOBILE LIFTS 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 Move 5 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 bc1aed16-c03c-46c5-9ebf-1a4ed3611b22 61 fields · synced May 22, 2026