← Back to catalogue
Viatom
EUDAMEDClass IIa (EU MDR)
Ref PO2Model PO2, PO4,PO2A,PO2B,PO2S,PO2C,PO2C-A,PO2C-S, PO4S,PO4C,PO4C-S
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 EUDAMEDPO2 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 69344401PO2ZG | Class IIa | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Shenzhen Viatom Technology Co., Ltd.
- 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