Skip to content

Lazarus Ponseti

by Kettering Surgical Appliances, Limited EUDAMED

Active European Union

Ref LP.AB.0.LModel LP.GR.S.000000

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number506068570LAZARAX Basic UDI-DIDate31 Jul 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Model / Reference
LP.GR.S.000000, LP.AB.0.L
Primary DI / UDI-DI
05060685701031
Basic UDI-DI
506068570LAZARAX
EMDN Code
Y061203,Y06120601
Device Class
Class I
Market of Registration
Ireland

Manufacturer details

EUDAMED SRN
UK-MF-000039578
Authorised representative
Kettering Surgical (Ireland) Limited IE-AR-000047560

Other devices from Kettering Surgical Appliances, Limited

See all devices from Kettering Surgical Appliances, Limited →

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