Tourni-S CH50

Ref TourniS.SK.CH.50Model Tourni-S

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number54300030690001B9 Basic UDI-DI 05430003069066UDI-DI	Date3 Jun 2026Registered	StatusActive

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name: Tourniquet
Model / Reference: Tourni-S, TourniS.SK.CH.50

Primary DI / UDI-DI: 05430003069066
Basic UDI-DI: 54300030690001B9
EMDN Code: V9003 Tourniquets

Device Class: Class I
EU market of registration: Belgium

Manufacturer details

EUDAMED SRN: BE-MF-000000332

Other devices from Idenpro bv

Tourni-S 200

Class I
Tourni-S 50

Class I

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