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Škrtidlo gumové

EUDAMED

Class I (EU MDR)

Ref P31554

by WWW.KOMPRESS.SK, s.r.o.

Identity

Device Name
Škrtidlo gumové EUDAMED
Model / Reference
P31554 EUDAMED

Identifiers

Primary DI / UDI-DI
08586029160373 EUDAMED
Basic UDI-DI
8586029160519A7 EUDAMED
EMDN Code
V9003 TOURNIQUETS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Slovakia 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

Škrtidlo gumové by WWW.KOMPRESS.SK, s.r.o. — 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
SK-MF-000053588

Sources (1)

  • EUDAMED 39a1d125-cfbf-46d4-9776-ef0c739fc58e 61 fields · synced Jul 9, 2026