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Teknogas

EUDAMED

Class IIb (EU MDR)

Ref VT50CFA

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

Identity

Trade Name
TEKNOGAS EUDAMED
Device Name
TEKNOGAS Octafluoropropane C3F8 50ml EUDAMED
Model / Reference
VT50CFA EUDAMED

Identifiers

Primary DI / UDI-DI
08680548905221 EUDAMED
Basic UDI-DI
B-08680548905221 EUDAMED
EMDN Code
Q02030101 INTRAOCULAR FLUORINATED DERIVATIVES EUDAMED

Classification

Device Class
Class IIb 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

Teknogas by TEKNOMEK MEDİKAL MALZEMELERİ SAN. ve TİC. LTD. ŞTİ. — Class IIb — 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 d4f185d6-1348-440d-a3dc-4f4a7ef319e5 61 fields · synced Jun 19, 2026