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

EUDAMED

Class I (EU MDR)

Ref 002

by Nanjing Kangju Medical Instrument Co., Ltd

Identity

Device Name
KJ-501 KJ-507 KJ-502 KJ-508 KJ-505 KJ-506 EUDAMED
Model / Reference
002 EUDAMED

Identifiers

Primary DI / UDI-DI
06974600320049 EUDAMED
Basic UDI-DI
69746003200UR EUDAMED
EMDN Code
C9005 PHONENDOSCOPES AND STETHOSCOPES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

Yes

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Kj-501 Kj-507 Kj-502 Kj-508 Kj-505 Kj-506 by Nanjing Kangju Medical Instrument Co., Ltd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

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

Sources (1)

  • EUDAMED f5e51e94-203c-4736-bacf-6d80e238f1ba 61 fields · synced Oct 6, 2026