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Vacusera

EUDAMED

Class IIa (EU MDR)

Ref 2392815N

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

Identity

Trade Name
VACUSERA EUDAMED
Device Name
VACUSERA® Pressure Activated Safety Blood Lancet EUDAMED
Model / Reference
2392815N EUDAMED

Identifiers

Primary DI / UDI-DI
+M7122392815N1+ EUDAMED
Basic UDI-DI
++M712239LANCETE8 EUDAMED
Direct Marketing DI
+M7122392815N1+ EUDAMED
EMDN Code
V010401 LANCETS WITH SAFETY SYSTEMS, SINGLE-USE 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

Category: Blood lancet, single-use

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

Similar devices

Also classified as Blood lancet, single-use.

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 cd363902-0739-4eab-9b2b-4bb47b8bf89f 61 fields · synced Jun 19, 2026