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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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Farmamed Soletta fascite plantare/Plant… — 2 UDI-DI variants, MDR

MD Atlas
Gabbiano S.p.A.

Data from EUDAMED, last updated May 31, 2026

Farmamed Soletta fascite plantare/Plantilla Fascitis Plantar 36/41

803256811M05472QP

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Gabbiano S.p.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 803256811M05472QP
Device name: Farmamed Soletta fascite plantare/Plantilla Fascitis Plantar 36/41
Device model: Soletta fascite plantare 36/41
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 29, 2025

Manufacturer & authorised representative

Manufacturer

Name: Gabbiano S.p.A.
SRN: IT-MF-000020347
Country: Italy
Email: info@gabbianospa.com
Phone: +39 0376283211

Variants by status

UDI-DI variants

2 UDI-DI variants

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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

0547208023766054720
0547308023766054737