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Protac KneedMe

by Protac A/S Denmark EUDAMED

Ref 700-751-3820-40, 700-755-U-3820-40, 700-755-U-3820-30 EMDN Y99

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number571488270075FV Basic UDI-DIDate10 Aug 2023RegisteredStatusActive

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  • Withdrawn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 · synced 22 Oct 2026

Trade Name
Protac KneedMe
Protac KneedMe To Go
Model / Reference
700-751-3820-40, 700-755-U-3820-40, 700-755-U-3820-30
Primary DI / UDI-DI
05714882012970, 05714882013052, 05714882013038
Basic UDI-DI
571488270075FV
Direct Marketing DI
05714882012970
05714882013052
05714882013038
EMDN Code
Y99 Devices for persons with disabilities not included in other categories - other
Device Class
Class I
Market of Registration
Denmark

Manufacturer details

EUDAMED SRN
DK-MF-000000963

Other devices from Protac A/S

See all devices from Protac A/S →

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 (3)

  • EUDAMED 6c262489-c922-476e-a3b2-22749eda5906 61 fields · synced 22 Oct 2026
  • EUDAMED 05714882013052|571488270075FV 61 fields · synced 17 May 2026
  • EUDAMED 05714882013038|571488270075FV 61 fields · synced 17 May 2026