Skip to content

Kaps FOOT MORNING: PROTECTUBE

by Laboratorios Herbitas, S.L. EUDAMED

Active European Union

Ref 103_2015_S / KAPS 6011.6

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number84351355RIZOUE Basic UDI-DIDate16 Oct 2024RegisteredStatusActive

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  • Withdrawn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
Tubo Gel Rizo
Model / Reference
103_2015_S / KAPS 6011.6
Primary DI / UDI-DI
08436534057678
Basic UDI-DI
84351355RIZOUE
EMDN Code
Y061203 Orthoses, foot (including insoles and inserts)
Device Class
Class I
Market of Registration
Poland

Manufacturer details

EUDAMED SRN
ES-MF-000004599

Other devices from Laboratorios Herbitas, S.L.

See all devices from Laboratorios Herbitas, S.L. →

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