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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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Organization name
UDI-DI code
Reference / catalog number

05472 — Class I MDR by Gabbiano S.p.A.

MD Atlas
Gabbiano S.p.A.

EUDAMED last updated this device on Sep 29, 2025

05472

803256811M05472QP

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Gabbiano S.p.A.
UDI-DI code: 08023766054720
Reference / catalog number: 05472

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View device family (Basic UDI)

Manufacturer information

Organization name: Gabbiano S.p.A.
SRN: IT-MF-000020347
Manufacturer status: Active

Related devices

Farmamed Bandage en filet tubulaire803256811M05401PYOn the market 05413803256811M05413Q7On the market 05512803256811M05417QFOn the market Farmamed Pansement Aqua No Problem avec protection bactériostatiqueB-08023766053235On the market Farmamed Pansement Articulations avec protection bactériostatiqueB-08023766053259On the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Italy; available across 2 countries total.

Country	On market since	Until
ItalyPrimary placement	Aug 1, 2023	Still on market
Spain	Aug 1, 2023	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08023766054720
Basic UDI-DI: 803256811M05472QP
Reference / catalog number: 05472
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 2
Additional product description: La soletta Farmamed è stata studiata per alleviare e prevenire l’insorgere della fascite plantare. I materiali con cui è realizzata, caratterizzati da spessori e densità diversificati, garantiscono un adeguato sostegno alle varie zone del piede, evitando di sovraccaricare la fascia plantare. Uno speciale inserto in fibra di alluminio sostiene e protegge la zona centrale del piede e dell’arco plantare. Il tessuto, realizzato con tecnologia FIR, contribuisce a migliorare la microcircolazione sanguigna.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08023766054720

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Y061203ORTHOSES, FOOT (INCLUDING INSOLES AND INSERTS)

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

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