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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

DAIA0000030 — IVDR Class A IVDR by Danaus S.r.l.

MD Atlas
Danaus S.r.l.

EUDAMED last updated this device on May 23, 2026

DAIA0000030

805792084DAIA0000030STN

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Danaus S.r.l.
UDI-DI code: 08057920840102
Reference / catalog number: DAIA0000030

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View device family (Basic UDI)

Manufacturer information

Organization name: Danaus S.r.l.
SRN: IT-MF-000054492
Manufacturer status: Active

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DAMA0000065805792084DAIA0000030STNOn the market DAMA0000086805792084DAIA0000030STNOn the market DAIA0000030S805792084DAIA0000030STNOn the market DANA0000010\C805792084DAIA0000030STNOn the market DANA0000005\C805792084DAIA0000030STNOn 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 1 country total.

Country	On market since	Until
ItalyPrimary placement	Jan 1, 2020	Jan 1, 2027

Device identification

Trade name: not provided
UDI-DI code: 08057920840102
Basic UDI-DI: 805792084DAIA0000030STN
Reference / catalog number: DAIA0000030
Issuing entity: GS1

Classification

Risk category: IVDR Class A
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Dispositivo mobile destinato alla conservazione in sicurezza e al trasporto di reagenti, campioni chimici, materiali di scarto e sostanze volatili potenzialmente nocive in ambiente di laboratorio diagnostico in vitro, mediante sistema di aspirazione e filtrazione molecolare integrato e disinfezione tramite raggi ultravioletti con lunghezza d’onda di 253,7 nm con protezione integrata per lo sversamento accidentale. Il dispositivo è destinato a prevenire l'esposizione degli operatori sanitari e la contaminazione dell'ambiente di laboratorio da vapori tossici e nocivi e sversamenti accidentali. La protezione è garantita da un sistema a flusso d'aria forzato continuo che convoglia i gas esausti verso un gruppo di filtrazione molecolare integrato a carboni attivi purificando l'aria prima della sua immissione nell'ambiente.
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

EMDN nomenclature code(s)

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

W02070304CHEMICAL FILTRATION AIR CLOSETS

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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