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Patient monitor

EUDAMED

Class IIb (EU MDR)

Ref M12

by Guangdong Biolight Meditech Co., Ltd

Identity

Trade Name
Patient monitor EUDAMED
Device Name
Patient monitor EUDAMED
Model / Reference
M12 EUDAMED

Identifiers

Primary DI / UDI-DI
06932562300110 EUDAMED
Basic UDI-DI
69325623100194C EUDAMED
EMDN Code
Z1203020201 MULTI–PARAMETER PATIENT BEDSIDE MONITORS EUDAMED

Classification

Device Class
Class IIb 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

Patient monitor by Guangdong Biolight Meditech Co., Ltd — Class IIb — 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 0b01f7f3-8e26-4429-8b0e-6f70bd015927 61 fields · synced May 23, 2026