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Hemostatic Tourniquet DNIPRO

EUDAMED

Class I (EU MDR)

Ref Hemostatic Tourniquet DNIPRO

by Limited Liability Company "manufacturing Company Prostir"

Identity

Device Name
Hemostatic Tourniquet DNIPRO EUDAMED
Model / Reference
Hemostatic Tourniquet DNIPRO EUDAMED

Identifiers

Primary DI / UDI-DI
04820261140613 EUDAMED
Basic UDI-DI
0482026114TQDniproJG EUDAMED
EMDN Code
V9003 TOURNIQUETS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Czechia 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

Hemostatic Tourniquet DNIPRO by Limited Liability Company "manufacturing Company Prostir" — 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
UA-MF-000039898
Authorised Representative
AFINA, spol.s r.o. CZ-AR-000000584

Sources (1)

  • EUDAMED 3a889ae3-1ed2-4909-87b9-840630d8de59 61 fields · synced Jun 19, 2026