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Electric wheelchair

EUDAMED

Class I (EU MDR)

Ref WT-100W(6001)Model WT-100W(6001)、WT-100W(6001A)、 WT-100W(6001B)、WT-100W(6002)、WT-100W(6002A)、WT-100W(6002B)、WT-100W(6003)、WT-100W(6004)、WT-100W(6005)、WT-100W(6005A)、WT-100W(6006)、WT-100W(6006A)、WT-100W(6006B)、WT-100W(6006C)、WT-100W(6007)、etcRef GM172

by Anhui Gmed Technology Co., Ltd.

Identity

Device Name
Electric wheelchair EUDAMED
Model / Reference
WT-100W(6001)、WT-100W(6001A)、 WT-100W(6001B)、WT-100W(6002)、WT-100W(6002A)、WT-100W(6002B)、WT-100W(6003)、WT-100W(6004)、WT-100W(6005)、WT-100W(6005A)、WT-100W(6006)、WT-100W(6006A)、WT-100W(6006B)、WT-100W(6006C)、WT-100W(6007)、etc EUDAMED
WT-100W(6001) EUDAMED
GM172 EUDAMED

Identifiers

Primary DI / UDI-DI
06977808140006 EUDAMED
06977808141089 EUDAMED
Basic UDI-DI
697780814wheelchair001TZ EUDAMED
EMDN Code
Y122127 ELECTRIC WHEELCHAIRS 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

Electric wheelchair by Anhui Gmed 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-000044045
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (2)

  • EUDAMED 0152a853-de77-4abb-b600-adb97424e2de 61 fields · synced Aug 1, 2026
  • EUDAMED d768ceb9-0633-4feb-bdbb-bd24d46c30cf 61 fields · synced Aug 1, 2026