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Gel Aphte Repair

EUDAMED

Class I (EU MDR)

Ref 8029408130647

by UNIFARCO SpA

Identity

Trade Name
Gel Aphte Repair EUDAMED
Device Name
GEL APHTE REPAIR FR EUDAMED
Model / Reference
8029408130647 EUDAMED

Identifiers

Primary DI / UDI-DI
D-FPGAFT10FEY EUDAMED
Basic UDI-DI
B-FPGAFT10FEY EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

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

Category: Device sterilization/disinfection container, reusable

Gel Aphte Repair by UNIFARCO SpA — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
UNIFARCO SpA
EUDAMED SRN
IT-MF-000013304

Sources (1)

  • EUDAMED dfb4c179-ce5c-45dc-9a39-74f41f30fcd9 61 fields · synced Aug 5, 2026