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Gel Aphthe Repair

EUDAMED

Class I (EU MDR)

Ref 8029408130623

by UNIFARCO SpA

Identity

Trade Name
Gel Aphthe Repair EUDAMED
Device Name
GEL APHTHE REPAIR DACH EUDAMED
Model / Reference
8029408130623 EUDAMED

Identifiers

Primary DI / UDI-DI
D-FPGAFT10TFU EUDAMED
Basic UDI-DI
B-FPGAFT10TFU EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

Gel Aphthe Repair by UNIFARCO SpA — Class I — 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
UNIFARCO SpA
EUDAMED SRN
IT-MF-000013304

Sources (1)

  • EUDAMED dce34fb2-758a-4013-89eb-d3444d96b50e 61 fields · synced Jul 28, 2026