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KEYLOCK™ Single Use Tourniquet

EUDAMED

Class I (EU MDR)

Ref GAR022

by GA Health Company Limited

Identity

Trade Name
KEYLOCK™ Single Use Tourniquet EUDAMED
Device Name
Tourniquet EUDAMED
Model / Reference
GAR022 EUDAMED

Identifiers

Primary DI / UDI-DI
14897106954169 EUDAMED
Basic UDI-DI
489710695GAR022FC EUDAMED
EMDN Code
V9003 TOURNIQUETS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Ireland 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

KEYLOCK™ Single Use Tourniquet by Ga Health Company Limited — 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
HK-MF-000019784
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 4577ef9d-cbcd-4232-82a4-fed4ea50241c 61 fields · synced Jun 19, 2026