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Pulse Oximeters

by Shenzhen Acurio Instrument Co., Ltd

Ref 93/42/EEC ON MEDICAL DEVICESModel AS-302-L

Active European Union

CE MDD

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-06939823801034 Basic UDI-DI 06939823801034UDI-DIDate25 Jun 2026RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
Fingertip Pulse Oximeter
Model / Reference
AS-302-L, 93/42/EEC ON MEDICAL DEVICES
Primary DI / UDI-DI
06939823801034
Basic UDI-DI
B-06939823801034
EMDN Code
Z1203020408 Pulse oximeters
Device Class
Class IIb
EU market of registration
France

Manufacturer details

EUDAMED SRN
CN-MF-000024296
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

Other devices from Shenzhen Acurio Instrument Co., Ltd

Properties

  • Measuring Function

Other properties (10)

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