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iFIT Prosthesis

by iFIT Prosthetics United States EUDAMED

Ref TT200TLiModel TT200

EMDN Y062409

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0850049686TT200i64 Basic UDI-DIDate15 Mar 2023RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
International KIT - Transtibial prosthetic device
Model / Reference
TT200, TT200TLi
Primary DI / UDI-DI
00850049686198
Basic UDI-DI
0850049686TT200i64
Direct Marketing DI
00850049686198
EMDN Code
Y062409 Transtibial prostheses (for amputation under knee)
Device Class
Class I
Market of Registration
Northern Ireland

Manufacturer details

EUDAMED SRN
US-MF-000032928
Authorised representative
Eurolink Europe Compliance Limited IE-AR-000002852

Other devices from iFIT Prosthetics

See all devices from iFIT Prosthetics →

Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED 7a346c52-49d2-41b0-8af3-718168823663 61 fields · synced 24 Oct 2026