← Back to catalogue

Walking stick

EUDAMED

Class I (EU MDR)

Ref F028Model F217 F216 F215 F308 F035 F036 F212 F214 F211 F406 F409 F213 F407 F028 F025 F031 F029 F210 F037 F307 F316 F306 F305 F207 F203 F017 F202 F204 F200 F019 F018 F206 F208 F027 F011 F013 F001 F004 F026 F030 F300 F500 F505 F650 F651 F652 F800 F209

by Ningbo Shenyu Medical Equipment Co., Ltd

Identity

Device Name
Walking stick EUDAMED
Model / Reference
F217 F216 F215 F308 F035 F036 F212 F214 F211 F406 F409 F213 F407 F028 F025 F031 F029 F210 F037 F307 F316 F306 F305 F207 F203 F017 F202 F204 F200 F019 F018 F206 F208 F027 F011 F013 F001 F004 F026 F030 F300 F500 F505 F650 F651 F652 F800 F209 EUDAMED
F028 EUDAMED

Identifiers

Primary DI / UDI-DI
06950572860288 EUDAMED
Basic UDI-DI
695057286028JS EUDAMED
EMDN Code
Y120303 WHITE STICKS FOR BLIND PERSONS 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

Walking stick by Ningbo Shenyu Medical Equipment 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

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

Manufacturer

EUDAMED SRN
CN-MF-000003330
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED 903e9bee-ab59-4a15-b017-e958b510982d 61 fields · synced Oct 6, 2026