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Torque Device

by TERUMO Medical Products(Hangzhou) Co., Ltd., EUDAMED

Active European Union

Ref XX*RF02MH

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69276755TDJM Basic UDI-DIDate5 Oct 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

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

Specification

EUDAMED

Device Name
RADIFOCUS Torque Device
Model / Reference
XX*RF02MH
Primary DI / UDI-DI
06927675513496
Basic UDI-DI
69276755TDJM
EMDN Code
C0480 Cardiovascular guidewires - accessories
Device Class
Class I
Market of Registration
Belgium

Manufacturer details

EUDAMED SRN
CN-MF-000001640
Authorised representative
TERUMO EUROPE N.V. BE-AR-000001433

Other devices from Terumo Medical Products (Hangzhou) Co., Ltd.

See all devices from Terumo Medical Products (Hangzhou) Co., Ltd. →

Properties

  • Sterile

Other properties (12)

  • 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