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GOT C3F8 multi

EUDAMED

Class IIb (EU MDR)

Ref GOT 009-01

by Al.chi.mi.a. S.r.l.

Identity

Trade Name
GOT C3F8 multi EUDAMED
Device Name
GOT C3F8 multi EUDAMED
Model / Reference
GOT 009-01 EUDAMED

Identifiers

Primary DI / UDI-DI
08021118001491 EUDAMED
Basic UDI-DI
B-08021118001491 EUDAMED
EMDN Code
Q02030101 INTRAOCULAR FLUORINATED DERIVATIVES EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

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

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

GOT C3F8 multi by Al.chi.mi.a. S.r.l. — 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

Manufacturer
Al.chi.mi.a. S.r.l.
EUDAMED SRN
IT-MF-000028901

Sources (1)

  • EUDAMED c250e798-f6f1-467a-ada9-ee1918d6014d 61 fields · synced Jul 15, 2026