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Tourniquet

EUDAMED

Class I (EU MDR)

Ref TOT600

by Medsource Factory, Inc.

Identity

Trade Name
Tourniquet EUDAMED
Device Name
Tourniquet EUDAMED
Model / Reference
TOT600 EUDAMED

Identifiers

Primary DI / UDI-DI
06975293690020 EUDAMED
Basic UDI-DI
697529369TOT600Z8 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

Category: Limb tourniquet, manual, reusable

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

Similar devices

Also classified as Limb tourniquet, manual, reusable.

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 c2b3d6a6-ade5-4142-a671-abfd5f38efb5 61 fields · synced Jun 19, 2026