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Vacusera

EUDAMED

Class I (EU MDR)

Ref 259001-2

by Di̇sera Tibbi̇ Malzeme Loji̇sti̇k San. Ve Ti̇c. A.ş.

Identity

Trade Name
VACUSERA EUDAMED
Device Name
VACUSERA® Automatic Tourniquet EUDAMED
Model / Reference
259001-2 EUDAMED

Identifiers

Primary DI / UDI-DI
+M712259001217 EUDAMED
Basic UDI-DI
++M712259ATOURNIQUETU6 EUDAMED
Direct Marketing DI
+M712259001217 EUDAMED
EMDN Code
V9003 TOURNIQUETS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Türkiye 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

Vacusera by Di̇sera Tibbi̇ Malzeme Loji̇sti̇k San. Ve Ti̇c. A.ş. — 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
TR-MF-000025066

Sources (1)

  • EUDAMED d07bb4c5-389f-4855-aae7-cc87bd250d4d 61 fields · synced Jun 18, 2026