Skip to content

1C62 Triton H, R, without footshell

by Otto Bock HealthCare LP EUDAMED

Active European Union

Ref 1C62=R24-2-2-P/0Model 1C62

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number406440900000000001C62RU Basic UDI-DIDate4 Sep 2026RegisteredStatusActive

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  • Withdrawn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

Device Name
1C62 Triton H, L, normal, light brown
Model / Reference
1C62, 1C62=R24-2-2-P/0
Primary DI / UDI-DI
04064409035861
Basic UDI-DI
406440900000000001C62RU
EMDN Code
Y062409 Transtibial prostheses (for amputation under knee)
Device Class
Class I
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
US-MF-000019567
Authorised representative
Ottobock SE & Co. KGaA DE-AR-000016531

Other devices from Otto Bock HealthCare LP

See all devices from Otto Bock HealthCare LP →

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