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: 06974576183327 EUDAMED
Basic UDI-DI: 697457618CrutchesDR EUDAMED
EMDN Code: Y12030601 ELBOW CRUTCHES EUDAMED

Classification

Device Class: Class I EUDAMED
Market of Registration: Austria EUDAMED

Clinical & Handling

Sterile

EUDAMED

Implantable

EUDAMED

Reusable

EUDAMED

Contains Latex

EUDAMED

Reprocessed

EUDAMED

CMR Substance

EUDAMED

Human-derived

EUDAMED

Human Tissues

EUDAMED

Animal Tissues

EUDAMED

Endocrine Disruptor

EUDAMED

Administering Medicine

EUDAMED

Measuring Function

EUDAMED

Incorporates Medicinal Product

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

Source	Region	Type	Cert / Approval No.	Class	Status
EUDAMED	European Union	CE/MDR	697457618CrutchesDR	Class I	Active

Is this your device? Claim it to add documentation and request validation.

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 9d76afdd-9f64-4e79-b45b-357bd44d7651 61 fields · synced Oct 6, 2026
EUDAMED 9d76afdd-9f64-4e79-b45b-357bd44d7651-1 61 fields · synced Jun 10, 2026