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Hema-T

EUDAMED

Class I (EU MDR)

Ref PRHS-30-80-T

by Oneg HaKarmel Ltd

Identity

Trade Name
Hema-T EUDAMED
Device Name
Hema-T EUDAMED
Model / Reference
PRHS-30-80-T EUDAMED

Identifiers

Primary DI / UDI-DI
7290012685187YA EUDAMED
Basic UDI-DI
729001268HEMAT7Q EUDAMED
Direct Marketing DI
7290012685187YA 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

Hema-T 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 691cd3db-b72a-4438-8ca3-4eee088220c0 61 fields · synced Jul 9, 2026