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HemaShock EMS

EUDAMED

Class I (EU MDR)

Ref PRHS-EM-01A

by Oneg HaKarmel Ltd

Identity

Trade Name
HemaShock EMS EUDAMED
Device Name
HemaShock EUDAMED
Model / Reference
PRHS-EM-01A EUDAMED

Identifiers

Primary DI / UDI-DI
7290012685439YE EUDAMED
Basic UDI-DI
729001268HEMASHOCK9L EUDAMED
Direct Marketing DI
7290012685439YE EUDAMED
EMDN Code
V9003 TOURNIQUETS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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

HemaShock EMS by Oneg Hakarmel Ltd — 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

Manufacturer
Oneg HaKarmel Ltd
EUDAMED SRN
IL-MF-000028966
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 6b163b56-d2e5-4ea1-96ed-91c8752d735e 61 fields · synced Jun 17, 2026