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Vacusera

EUDAMED

Class IIa (EU MDR)

Ref 24125190GM

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

Identity

Trade Name
VACUSERA EUDAMED
Device Name
VACUSERA® Blood Collection Set EUDAMED
Model / Reference
24125190GM EUDAMED

Identifiers

Primary DI / UDI-DI
+M71224125190GM17 EUDAMED
Basic UDI-DI
++M712241BLOODCSETBM EUDAMED
Direct Marketing DI
+M71224125190GM17 EUDAMED
EMDN Code
A01010201 BUTTERFLY NEEDLES, WITH SAFETY SYSTEMS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

Yes

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

Vacusera by Di̇sera Tibbi̇ Malzeme Loji̇sti̇k San. Ve Ti̇c. A.ş. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

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 a1b968d1-6079-4af8-ab60-d386d0c81225 61 fields · synced Jun 18, 2026