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Patient Lift

EUDAMED

Class I (EU MDR)

Ref T-FLEXModel T-FLEX, MINI, MN-6219, MY101, MY201, MY302, MY108, MY106, MN776, MN777, MN-HY801, MN-HY803, MN-003A, MN-001A

by Chongqing Muniu Power Technology Co., Ltd

Identity

Device Name
Patient Lift EUDAMED
Model / Reference
T-FLEX, MINI, MN-6219, MY101, MY201, MY302, MY108, MY106, MN776, MN777, MN-HY801, MN-HY803, MN-003A, MN-001A EUDAMED
T-FLEX EUDAMED

Identifiers

Primary DI / UDI-DI
16976578617104 EUDAMED
Basic UDI-DI
697657861PatientLift710GG EUDAMED
EMDN Code
V080502 PATIENT TRANSFER CHAIRS 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 Chongqing Muniu Power 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-000036515
Authorised Representative
Sungo Cert GmbH DE-AR-000010869

Sources (1)

  • EUDAMED d6c2e191-91d7-44d3-9654-2741a8b88304 61 fields · synced Jul 14, 2026