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Teknomek

EUDAMED

Class IIa (EU MDR)

Ref VT10D

by TEKNOMEK MEDİKAL MALZEMELERİ SAN. ve TİC. LTD. ŞTİ.

Identity

Trade Name
TEKNOMEK EUDAMED
Device Name
Perfluorodecalin 10ml vial EUDAMED
Model / Reference
VT10D EUDAMED

Identifiers

Primary DI / UDI-DI
08680548905320 EUDAMED
Basic UDI-DI
B-08680548905320 EUDAMED
EMDN Code
Q02030205 OPHTHALMIC SURGERY, PERFLUOROCARBONS PURE AND COMBINED WITH OTHER SUBSTANCES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Teknomek by TEKNOMEK MEDİKAL MALZEMELERİ SAN. ve TİC. LTD. ŞTİ. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
TR-MF-000018462

Sources (1)

  • EUDAMED 77f10bc8-a668-4371-93f8-2b0b644c5fff 61 fields · synced Jun 19, 2026