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Sonicaid

by ArjoHuntleigh AB EUDAMED

Active European Union

Ref SR2Model SRX

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5060693520358WM Basic UDI-DIDate7 Oct 2024RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

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.

Specification

EUDAMED

Device Name
Srx
Model / Reference
SRX, SR2
Primary DI / UDI-DI
05051968031693
Basic UDI-DI
5060693520358WM
EMDN Code
Z12080101 Foetal monitors
Device Class
Class IIa
Market of Registration
Ireland

Manufacturer details

EUDAMED SRN
SE-MF-000000696

Other devices from Arjohuntleigh AB

See all devices from Arjohuntleigh AB →

Properties

Other properties (13)

  • 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
  • Measuring Function: No
  • Incorporates Medicinal Product: No