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Altair 220 kg Kit Europe

EUDAMED

Class I (EU MDR)

Ref 55210-EU Model Altair

by Human Care HC AB

Identity

Trade Name
Altair 220 kg Kit Europe EUDAMED
Model / Reference
Altair EUDAMED
55210-EU EUDAMED

Identifiers

Primary DI / UDI-DI
07331599441459 EUDAMED
Basic UDI-DI
7331599LA55200H55220HY2 EUDAMED
EMDN Code
V08050399 PATIENT TRANSFER LIFTS - OTHER EUDAMED

Classification

Device Class
Class I 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

Altair 220 kg Kit Europe by Human Care HC 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
Human Care HC AB
EUDAMED SRN
SE-MF-000002090

Sources (1)

  • EUDAMED 7b4fc6d8-f4d8-4b14-86ef-794c7f785c73 61 fields · synced Jul 19, 2026