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Pulse Oximeter

by Shenzhen Viatom Technology Co., Ltd. 28 variants

Ref PO6BModel PO6B、PO6C

Pulse Oximeter (PO6B) is a medical device (EU MDD Class IIa; EMDN category pulse oximeters) made by Shenzhen Viatom Technology Co., Ltd., registered in EUDAMED on 21 Dec 2023 (Basic UDI-DI B-06934440102458), active as of 22 Oct 2026.

Active European Union

CE MDD

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/MDD NumberB-06934440102458 Basic UDI-DI 06934440102458UDI-DIDate21 Dec 2023RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Trade name
Wellue
Device name
Pulse Oximeter
Model / reference
PO6B, PO6B、PO6C
Primary DI / UDI-DI
06934440102458
Basic UDI-DI
B-06934440102458, 69344401PO6BRJ
Direct marketing DI
06934440102458
EMDN code
Z1203020408 Pulse oximeters
Device class
Class IIa
EU registration type
Legacy device (under a directive)
Standard device
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)