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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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MD Atlas
FOSHAN FEIYANG MEDICAL EQUIPMENT CO., LTD.

Data from EUDAMED, last updated Jun 11, 2026

WALKER

697594951WALKER4R

1 reference

Class I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk category: Class I
Manufacturer: FOSHAN FEIYANG MEDICAL EQUIPMENT CO., LTD.

Device family identification

Device name: WALKER
Basic UDI-DI: 697594951WALKER4R
Device model: FY912L
Issuing agency: GS1
Version date: Mar 10, 2025

Classification

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk category: Class I
Status: On the market

Manufacturer & authorised representative

Manufacturer

Name: FOSHAN FEIYANG MEDICAL EQUIPMENT CO., LTD.
SRN: CN-MF-000032043
Country: China
Email: fymed@vip.163.com

Authorised representative

Name: SUNGO Europe B.V.
SRN: NL-AR-000000247
Country: Netherlands

Device characteristics

No device characteristics flagged

EMDN code(s)

European Medical Device Nomenclature — the EU product classifications carried across this device family's references.

Y120603Walking frames, 4 tips

References by status

References

1 reference

Export results

Applied filters

basicUdiUlid01JP06XBW2N6CFVJE1QJE43BF0

Format

Summary

31 columns included

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
FY912L	`FY912L`	`06975949519934`	1	On the market