Electric Wheelchair

by Zhejiang Jianrui Technology Company Limited 4 variants

Ref JLE-W00A-2022Model JLE-W00A-2022 JLE-W01A-2023

Active European Union and United States

CE MDR 510(k)

Valid until

Not listed

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K240255↗

FDA record

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, FDA 510(k), synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k) 510(k)	NumberK240255	Date7 Aug 2024Issued	StatusActive
European Union	CE/MDR EUDAMED	Number697677817zjjrkjddlyc01C2 Basic UDI-DI 06976778170013UDI-DI	Date12 Oct 2023Registered	StatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

2 jurisdictions

Active
Expiring
Withdrawn
Listed
Not covered

United States FDA 510(k) Active
European Union CE/MDR Active

Specification

EUDAMED · 510(k)

Device Name: Electric Wheelchair
Model / Reference: JLE-W00A-2022 JLE-W01A-2023, JLE-W00A-2022

Primary DI / UDI-DI: 06976778170013
Basic UDI-DI: 697677817zjjrkjddlyc01C2
EMDN Code: Y122127 Electric wheelchairs

Device Class: Class I
EU market of registration: Austria

Manufacturer details

EUDAMED SRN: CN-MF-000037847
Authorised representative: SUNGO Europe B.V. NL-AR-000000247

Other devices from Zhejiang Jianrui Technology Company Limited

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