folding walking frames

by Zhongshan A&E Machinery Industry Co., Ltd. 4 variants

Ref 230 ELModel 230； 230 EL； 233 EL； 233 ELC

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number697789798foldingwalkingZ4 Basic UDI-DI 06977897980019UDI-DI	Date4 Nov 2024Registered	StatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name: folding walking frames
Model / Reference: 230； 230 EL； 233 EL； 233 ELC, 230 EL

Primary DI / UDI-DI: 06977897980019
Basic UDI-DI: 697789798foldingwalkingZ4
EMDN Code: Y120603 Walking frames, 4 tips

Device Class: Class I
Market of Registration: Austria

Manufacturer details

EUDAMED SRN: CN-MF-000038650
Authorised representative: SUNGO Europe B.V. NL-AR-000000247

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Properties

Other properties (13)

Sterile: No
Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
CMR Substance: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Endocrine Disruptor: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No