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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

2020 — Class IIa MDR by FARMA-DERMA S.r.l.

MD Atlas
FARMA-DERMA S.r.l.

EUDAMED last updated this device on May 28, 2026

2020

803259587TF07EP

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: FARMA-DERMA S.r.l.
UDI-DI code: 08032595871385
Reference / catalog number: 2020

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View device family (Basic UDI)

Manufacturer information

Organization name: FARMA-DERMA S.r.l.
SRN: IT-MF-000020737
Manufacturer status: Active

Critical warnings

8 warnings recorded — scroll inside the panel to see all entries.

CW999
Instructions for use and warnings: read the inside package insert.
CW999
WARNINGS AND PRECAUTIONS Avoid contact with eyes.
CW007
Do not use after the expiry date or if the pack is open or damaged.
CW135
WARNINGS AND PRECAUTIONS Keep out of the reach of children.
CW999
CONTRAINDICATIONS Do not use in case of individual hypersensitivity to one of the components of the product.
CW999
UNDESIRED EFFECTS Use of all products for topical use, especially if prolonged, may cause sensitisation. In that case, or if other undesired effects occur, stop treatment and consult your doctor or pharmacist.
CW275
In case of pregnancy or breastfeeding consult the doctor before using the device.
CW032
Do not use after the expiry date or if the pack is open or damaged.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	Apr 25, 2025	Dec 19, 2027

Device identification

Trade name: not provided
UDI-DI code: 08032595871385
Basic UDI-DI: 803259587TF07EP
Reference / catalog number: 2020
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: Indications: IALOCLEAN spray for oropharyngeal mucosa is indicated as adjuvant treatment of respiratory tract diseases due to oropharyngitis both in the acute and chronic phase, flu or cold syndromes, gastric reflux.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: Adulti e bambini di 2 anni / Adults and children from 2 years of age

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08032595871385

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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.

Q0399ENT DEVICES - OTHER

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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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.