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Tourniquet

EUDAMED

Class I (EU MDR)

Ref TOT2000

by Medsource Factory, Inc.

Identity

Trade Name
Tourniquet EUDAMED
Device Name
Tourniquet EUDAMED
Model / Reference
TOT2000 EUDAMED

Identifiers

Primary DI / UDI-DI
06975293690013 EUDAMED
Basic UDI-DI
697529369TOT200077 EUDAMED
EMDN Code
V9003 TOURNIQUETS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Tourniquet by Medsource Factory, Inc. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000047853
Authorised Representative
MedPath GmbH DE-AR-000000087

Sources (1)

  • EUDAMED 46f807f3-ca8d-4c77-93a1-e02c6780da2f 61 fields · synced Jul 24, 2026