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Protac MyFit (KK)

by Protac A/S EUDAMED

Withdrawn No longer placed on the EU market

Ref 800-821-10-B_KK

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number57148828008TX Basic UDI-DIDate21 Jun 2023RegisteredStatusWithdrawn No longer placed on the EU market

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Withdrawn

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Protac MyFit
Model / Reference
800-821-10-B_KK
Primary DI / UDI-DI
05714882013540
Basic UDI-DI
57148828008TX
Direct Marketing DI
05714882013540
EMDN Code
Y99 Devices for persons with disabilities not included in other categories - other
Device Class
Class I
Market of Registration
Sweden

Manufacturer details

EUDAMED SRN
DK-MF-000000963

Other devices from Protac A/S

See all devices from Protac A/S →

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