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RockTape® GO Standard Beige

by Implus Footcare United States EUDAMED

Ref 28473 EMDN M030402030102

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number3700006ROCKTAPEGOS4 Basic UDI-DIDate6 Jan 2026RegisteredStatusActive

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  • Withdrawn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

Device Name
RockTape® GO – Precut Kinesiology Tape
Model / Reference
28473
Primary DI / UDI-DI
03700006228473
Basic UDI-DI
3700006ROCKTAPEGOS4
EMDN Code
M030402030102 Elastic support bandages, adhesive extensible in one direction, high extensibility
Device Class
Class I
Market of Registration
France

Manufacturer details

EUDAMED SRN
US-MF-000050888
Authorised representative
IMPLUS EU FR-AR-000050172

Other devices from Implus Footcare

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 318bac4a-37d9-4a7c-b85c-b3f6ae1e62ad 61 fields · synced 22 Oct 2026