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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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GEL APHTE REPAIR FR — 1 UDI-DI variant, MDD (UNIFARCO SpA)

MD Atlas
UNIFARCO SpA

Data from EUDAMED, last updated May 30, 2026

GEL APHTE REPAIR FR

B-FPGAFT10FEY

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class I

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Manufacturer: UNIFARCO SpA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: B-FPGAFT10FEY
Device name: GEL APHTE REPAIR FR
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Version date: Jan 8, 2026

Manufacturer & authorised representative

Manufacturer

Name: UNIFARCO SpA
SRN: IT-MF-000013304
Country: Italy
Email: info@unifarco.it
Phone: +39 0437 806192

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KEF4F611VG118MG0XKFDA48F

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

Gel Aphte RepairD-FPGAFT10FEY