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Vacusera

EUDAMED

Class IIa (EU MDR)

Ref 260023K

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

Identity

Trade Name
VACUSERA EUDAMED
Device Name
VACUSERA® Blood Collection Needle EUDAMED
Model / Reference
260023K EUDAMED

Identifiers

Primary DI / UDI-DI
+M712260023K1L EUDAMED
Basic UDI-DI
++M712250NEEDLEAQ EUDAMED
Direct Marketing DI
+M712260023K1L EUDAMED
EMDN Code
A01010502 NEEDLES FOR COLLECTION UNDER VACUUM, W/O 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 5732f622-c4f1-4e76-9cab-d811c1dd584a 61 fields · synced Jun 19, 2026