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Life Rhythm

by Ritim Grup Tibbi Cihazlar Elektronik Sanayi Ve Ticaret Anonim Sirketi 17 variants

Ref LR-0233-0010Model AED-LR-0233-0010

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08682943411109 Basic UDI-DI 08682943411109UDI-DIDate14 Apr 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  • Withdrawn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
Life Rhythm AED Otomatik – Kapaklı – Ekransız - EN
Model / Reference
AED-LR-0233-0010, LR-0233-0010
Primary DI / UDI-DI
08682943411109
Basic UDI-DI
B-08682943411109
EMDN Code
Z12030503 Automatic defibrillators
Device Class
Class III
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000038675

Other devices from Ritim Grup Tibbi Cihazlar Elektronik Sanayi Ve Ticaret Anonim Sirketi

See all devices from Ritim Grup Tibbi Cihazlar Elektronik Sanayi Ve Ticaret Anonim Sirketi →

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