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Electrocardiograph

EUDAMED

Class IIa (EU MDR)

Ref E30

by Guangdong Biolight Meditech Co., Ltd

Identity

Trade Name
Electrocardiograph EUDAMED
Device Name
Electrocardiograph EUDAMED
Model / Reference
E30 EUDAMED

Identifiers

Primary DI / UDI-DI
06932562300547 EUDAMED
Basic UDI-DI
69325623100274B EUDAMED
EMDN Code
Z12050301 GENERAL PURPOSE ELECTROCARDIOGRAPHS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

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

Electrocardiograph by Guangdong Biolight Meditech 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-000006333
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED d25cd574-c05f-4158-b5c2-237cffec90da 61 fields · synced May 23, 2026