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Fingertip Pulse Oximeter

by Shenzhen Bsx Technology Electronics Co., Ltd. 2 variants

Ref REFModel BSX253,BSX233,BSX251,BSX255B,BSX238B,BSX231

Active European Union

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69204853BSXQ3R7 Basic UDI-DI 06920485307491UDI-DIDate14 Nov 2024RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Fingertip Pulse Oximeter
Model / Reference
BSX253, BSX233, BSX251, BSX255B, BSX238B, BSX231, REF
Primary DI / UDI-DI
06920485307491
Basic UDI-DI
69204853BSXQ3R7
Direct Marketing DI
06920485307491
EMDN Code
Z1203020408 Pulse oximeters
Device Class
Class IIa
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000015965
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

Other devices from Shenzhen Bsx Technology Electronics Co., Ltd.

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Properties

  • Measuring Function

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Incorporates Medicinal Product: No