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Crutches

EUDAMED

Class I (EU MDR)

Ref N/AModel SC1001/ SC1002/SC1003/SC1021/SC1022/SC1023/SC1001X/SC1031/SC1032/SC1033/SC1033SA-M/SC1033SA-L/SC1040S/SC1040DE/SC1040IT/SC2001/SC2011/SC2021/SC2031/SC2074/SC2031CA/SC2031C/SC3013/SC3020/SC3021/SC3030/SC3030F/SC3031/SCSC3101/SC3102/SC3203B-N,etc.

by Foshan Suncare Medical Products Co., Ltd

Identity

Device Name
Crutches EUDAMED
Model / Reference
SC1001/ SC1002/SC1003/SC1021/SC1022/SC1023/SC1001X/SC1031/SC1032/SC1033/SC1033SA-M/SC1033SA-L/SC1040S/SC1040DE/SC1040IT/SC2001/SC2011/SC2021/SC2031/SC2074/SC2031CA/SC2031C/SC3013/SC3020/SC3021/SC3030/SC3030F/SC3031/SCSC3101/SC3102/SC3203B-N,etc. EUDAMED
N/A EUDAMED

Identifiers

Primary DI / UDI-DI
06974576182245 EUDAMED
Basic UDI-DI
697457618CrutchesDR EUDAMED
EMDN Code
Y120399 WALKING DEVICES, ONE-HANDED OPERATION - OTHER 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

Crutches by Foshan Suncare Medical Products 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

Manufacturer
Foshan Suncare Medical Products Co., Ltd
EUDAMED SRN
CN-MF-000008985
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (2)

  • EUDAMED 75edc30c-3d9f-4ebd-b983-88eefa04014a 61 fields · synced Oct 7, 2026
  • EUDAMED 75edc30c-3d9f-4ebd-b983-88eefa04014a-1 61 fields · synced Jun 10, 2026