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Viatom

EUDAMED

Class IIa (EU MDR)

Ref PO2Model PO2, PO4,PO2A,PO2B,PO2S,PO2C,PO2C-A,PO2C-S, PO4S,PO4C,PO4C-S

by Shenzhen Viatom Technology Co., Ltd.

Identity

Trade Name
Viatom EUDAMED
Device Name
Pulse Oximeter EUDAMED
Model / Reference
PO2, PO4,PO2A,PO2B,PO2S,PO2C,PO2C-A,PO2C-S, PO4S,PO4C,PO4C-S EUDAMED
PO2 EUDAMED

Identifiers

Primary DI / UDI-DI
06934440102021 EUDAMED
Basic UDI-DI
69344401PO2ZG EUDAMED
Direct Marketing DI
06934440102021 EUDAMED
EMDN Code
Z1203020408 PULSE OXIMETERS 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

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Viatom by Shenzhen Viatom Technology 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-000012182
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 0e7bdb81-e72e-4727-9936-ba03a900b7c8 61 fields · synced Jun 15, 2026