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Cardidom

EUDAMED

Class IIa (EU MDR)

Ref LS802-GP

by Guangdong Transtek Medical Electronics Co., Ltd.

Identity

Trade Name
Cardidom EUDAMED
Device Name
Blood Pressure Monitor EUDAMED
Model / Reference
LS802-GP EUDAMED

Identifiers

Primary DI / UDI-DI
06932825304169 EUDAMED
Basic UDI-DI
69328253LS802GPM3 EUDAMED
Direct Marketing DI
06932825304169 EUDAMED
EMDN Code
Z1203020501 NON–INVASIVE OSCILLOMETRIC BLOOD PRESSURE GAUGES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France 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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Cardidom by Guangdong Transtek Medical Electronics Co., Ltd — Class IIa — 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-000010684
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (1)

  • EUDAMED 2540802a-7e87-432c-a1c1-d2c2754d7c60 61 fields · synced Jul 22, 2026