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ROLSELEY Silicone Tourniquet

by ROLSELEY Limited 16 variants

Ref M1C_SIL_CH_TealModel TNQ-T0K00

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number506057892TNQT0K008S Basic UDI-DI 05060578928200UDI-DIDate12 May 2026RegisteredStatusActive

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  • Withdrawn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 Active

Specification

EUDAMED

Device Name
Silicone Tourniquet
Model / Reference
TNQ-T0K00, M1C_SIL_CH_Teal
Primary DI / UDI-DI
05060578928200
Basic UDI-DI
506057892TNQT0K008S
EMDN Code
V9003 Tourniquets
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
GB-MF-000022778
Authorised representative
MB "Tikrola" LT-AR-000049108

Other devices from ROLSELEY Limited

See all devices from ROLSELEY Limited →

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