Kj-501 Kj-507 Kj-502 Kj-508 Kj-505 Kj-506

by Nanjing Kangju Medical Instrument Co., Ltd 6 variants

Ref 001

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	Number69746003200UR Basic UDI-DI 06974600320025UDI-DI	Date27 Mar 2025Registered	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Withdrawn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: Kj-501 Kj-507 Kj-502 Kj-508 Kj-505 Kj-506
Model / Reference: 001

Primary DI / UDI-DI: 06974600320025
Basic UDI-DI: 69746003200UR
Direct Marketing DI: 06974600320025
EMDN Code: C9005 Phonendoscopes and stethoscopes

Device Class: Class I
EU market of registration: Germany

Manufacturer details

EUDAMED SRN: CN-MF-000019114
Authorised representative: Sungo Cert GmbH DE-AR-000010869

Other devices from Nanjing Kangju Medical Instrument Co., Ltd

Blood pressure cuff

Class I
Kj-501 Kj-507 Kj-502 Kj-508 Kj-505 Kj-506

Class I
Kj-501 Kj-507 Kj-502 Kj-508 Kj-505 Kj-506

Class I
Kj-501 Kj-507 Kj-502 Kj-508 Kj-505 Kj-506

Class I
Kj-501 Kj-507 Kj-502 Kj-508 Kj-505 Kj-506

Class I
Kj-501 Kj-507 Kj-502 Kj-508 Kj-505 Kj-506

Class I

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