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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

I48V02430 — Class IIb MDR by ISTITUTO GANASSINI…

MD Atlas
ISTITUTO GANASSINI S.p.A. di Ricerche Biochimiche

EUDAMED last updated this device on May 4, 2026

I48V02430

805044485100020072

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: ISTITUTO GANASSINI S.p.A. di Ricerche Biochimiche
UDI-DI code: 08055510241469
Reference / catalog number: I48V02430

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View device family (Basic UDI)

Manufacturer information

Organization name: ISTITUTO GANASSINI S.p.A. di Ricerche Biochimiche
SRN: IT-MF-000027942
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Italy; available across 3 countries total.

Country	On market since	Until
ItalyPrimary placement		Still on market
Spain		Still on market
Romania		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08055510241469
Basic UDI-DI: 805044485100020072
Reference / catalog number: I48V02430
Issuing entity: GS1

Classification

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

Device details

Quantity: 18
Additional product description: Italian sales unit
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 5 MU03

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08055510241469

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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.

Q030103NASAL IRRIGATION SOLUTIONS

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.