Tourniquet

by Guangzhou Topmedi Co., Ltd. 5 variants

Ref E118Model TM-E112TO, TM-E112TBL, etc.

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

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number697438762TT001QL Basic UDI-DI 06974387624057UDI-DI	Date7 Nov 2023Registered	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Withdrawn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

Model / Reference: TM-E112TO, TM-E112TBL, etc., E118

Primary DI / UDI-DI: 06974387624057
Basic UDI-DI: 697438762TT001QL
EMDN Code: V9003 Tourniquets

Device Class: Class I
EU market of registration: France

Manufacturer details

EUDAMED SRN: CN-MF-000016883
Authorised representative: MedNet EC-REP GmbH DE-AR-000000002

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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