Pelvic Floor Rehabilitation Device

by Wuhan Kemaikang Technology Co., Ltd. 8 variants

Ref PD2603

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number697540909PD3Z Basic UDI-DI 06975409091406UDI-DI	Date4 Jul 2026Registered	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.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name: Pelvic Floor Rehabilitation Therapy Device
Model / Reference: PD2603

Primary DI / UDI-DI: 06975409091406
Basic UDI-DI: 697540909PD3Z
Direct Marketing DI: 06975409091406
EMDN Code: U070399 Pelvic floor rehabilitation devices - other

Device Class: Class IIa
EU market of registration: Germany

Manufacturer details

EUDAMED SRN: CN-MF-000056781
Authorised representative: AION CIRCUITS, LDA PT-AR-000044689

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Breast Pump

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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