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Patient Lift

EUDAMED

Class I (EU MDR)

Ref DH129016Model DH079008/DH079009/DH079010

by Foshan Dahao Medical Technology Co., Ltd.

Identity

Device Name
PATIENT LIFT EUDAMED
Model / Reference
DH079008/DH079009/DH079010 EUDAMED
DH129016 EUDAMED

Identifiers

Primary DI / UDI-DI
06973717274283 EUDAMED
Basic UDI-DI
697371727DHPLPL 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

Patient Lift by Foshan Dahao Medical Technology Co., 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

EUDAMED SRN
CN-MF-000035947
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED 41b9db0f-ca1d-4001-8cf7-0ee3195e46e3 61 fields · synced Oct 7, 2026