Tourniquet

by Qidong Yongsheng Medical Products Factory 8 variants

Ref TPE Type / 3702Model TPE Type, Synthetic Rubber Type, Polyester Type

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	Number697499300TourniquetDY Basic UDI-DI 16974993000075UDI-DI	Date30 Oct 2024Registered	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Withdrawn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: TPE Type, Synthetic Rubber Type, Polyester Type, TPE Type / 3702

Primary DI / UDI-DI: 16974993000075
Basic UDI-DI: 697499300TourniquetDY
EMDN Code: V9003 Tourniquets

Device Class: Class I
EU market of registration: Austria

Manufacturer details

EUDAMED SRN: CN-MF-000002913
Authorised representative: SUNGO Europe B.V. NL-AR-000000247

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Properties

Reprocessed

Other properties (12)

Sterile: No
Implantable: No
Reusable: No
Contains Latex: 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