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Pulse Oximeter

by Shenzhen Viatom Technology Co., Ltd. 28 variants

Ref PO6Model PO6、PO6A、 PO1、 PO1B

Pulse Oximeter (PO6) is a Class IIa device made by Shenzhen Viatom Technology Co., Ltd., registered in EUDAMED on 23 May 2026 (Basic UDI-DI 69344401PO6ZQ), active as of 22 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69344401PO6ZQ Basic UDI-DI 06934440102366UDI-DIDate23 May 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Pulse Oximeter
Model / reference
PO6、PO6A、 PO1、 PO1B, PO6
Primary DI / UDI-DI
06934440102366
Basic UDI-DI
69344401PO6ZQ, B-06934440102366
Direct marketing DI
06934440102366
EMDN code
Z1203020408 Pulse oximeters
Device class
Class IIa
EU registration type
Standard device
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000012182
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

Similar devices in this category

Other devices filed under PULSE OXIMETERS.

Other devices from Viatom Technology Co., Ltd.

See all devices from Viatom Technology Co., Ltd. →

Properties

  • Measuring function
Other properties (13, all answered No)