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SpO2 Extension Cable

EUDAMED

Class I (EU MDR)

Ref A0209-C02Ref 1032093

by APK Technology Co., Ltd.

Identity

Trade Name
SpO2 Extension Cable EUDAMED
Device Name
SpO2 Extension Cable EUDAMED
Model / Reference
A0209-C02 EUDAMED
1032093 EUDAMED

Identifiers

Primary DI / UDI-DI
06946725579329 EUDAMED
06946725569412 EUDAMED
Basic UDI-DI
69467255A-SPO2-cableKJ EUDAMED
EMDN Code
Z1203020285 MULTI-PARAMETER MONITORS - CONSUMABLES EUDAMED
Z12030285 VITAL SIGNS MONITORING INSTRUMENTS - CONSUMABLES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

EUDAMED

Contains Latex

No

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

SpO2 Extension Cable by APK Technology 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-000011581
Authorised Representative
Ruiyi Healthcare GmbH DE-AR-000005962

Sources (2)

  • EUDAMED 91a846c1-2db3-4994-9a12-e3cbc581f1cc 61 fields · synced Aug 1, 2026
  • EUDAMED d21a5d98-bbe7-4648-a09c-8e7b14bc4be8 61 fields · synced Aug 1, 2026