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Ardoo

EUDAMED

Class I (EU MDR)

Ref ACHO001Model ARDOOH01

by Polymorit Ltd

Identity

Trade Name
Ardoo EUDAMED
Device Name
Ardoo Caresafe 140 Hoist EUDAMED
Model / Reference
ARDOOH01 EUDAMED
ACHO001 EUDAMED

Identifiers

Primary DI / UDI-DI
05060225390176 EUDAMED
Basic UDI-DI
506022539ARDOOH01HR 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

Ardoo by Polymorit Ltd — 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
Polymorit Ltd
EUDAMED SRN
GB-MF-000024688
Authorised Representative
Eurolink Europe Compliance Limited IE-AR-000002852

Sources (1)

  • EUDAMED 76a329fb-ab14-493e-8d2d-2db8c7a6834e 61 fields · synced Jul 9, 2026