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Protac MyFit (KK)

by Protac A/S 10 variants

Ref 800-821-10-M/L_KK, 800-821-10-S_KK, 800-841-10-J_KK, 800-841-10-M/L_KK, 800-821-10-XL/2XL_KK, 800-821-10-J_KK

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDR, withdrawn

Ended

Withdrawn

Date not published (CE MDR)

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number57148828008TX Basic UDI-DI Date21 Jun 2023RegisteredStatusWithdrawn No longer placed on the EU market

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Withdrawn

Specification

EUDAMED

Device Name
Protac MyFit
Model / Reference
800-821-10-M/L_KK, 800-821-10-S_KK, 800-841-10-J_KK, 800-841-10-M/L_KK, 800-821-10-XL/2XL_KK, 800-821-10-J_KK
Primary DI / UDI-DI
05714882013588, 05714882013601, 05714882013748, 05714882013762, 05714882013625, 05714882013564
Basic UDI-DI
57148828008TX
Direct Marketing DI
05714882013588
05714882013601
05714882013748
05714882013762
05714882013625
05714882013564
EMDN Code
Y99 Devices for persons with disabilities not included in other categories - other
Device Class
Class I
EU 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