Pedal Exerciser

by Foshan Duson Medical Technology Co., Ltd.

Ref DS9001Model DS9001,DS9002,DS9003,DS9004,DS9005,DS9006,DS9007,DS9008,DS9009,DS9010

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number697792826PE01T3 Basic UDI-DI 06977928266235UDI-DI	Date28 Apr 2026Registered	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Withdrawn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: Pedal Exerciser
Model / Reference: DS9001, DS9002, DS9003, DS9004, DS9005, DS9006, DS9007, DS9008, DS9009, DS9010

Primary DI / UDI-DI: 06977928266235
Basic UDI-DI: 697792826PE01T3
EMDN Code: Y0504 Arms, torso and legs re-education devices

Device Class: Class I
EU market of registration: Austria

Manufacturer details

EUDAMED SRN: CN-MF-000044392
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