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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

URIGLASS KIT — IVDR Class A IVDR by BIOSIGMA S.P.A.

MD Atlas
BIOSIGMA S.P.A.

EUDAMED last updated this device on Mar 24, 2026

URIGLASS KIT

803367356URINALYSISX2

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: BIOSIGMA S.P.A.
UDI-DI code: 08033673560023
Reference / catalog number: U9028

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View device family (Basic UDI)

Manufacturer information

Organization name: BIOSIGMA S.P.A.
SRN: IT-MF-000030370
Manufacturer status: Active

Related devices

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Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Italy; available across 1 country total.

Placed on the market in Italy; per-country availability dates not published.

Device identification

Trade name: URIGLASS KIT
UDI-DI code: 08033673560023
Basic UDI-DI: 803367356URINALYSISX2
Reference / catalog number: U9028
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: 100
Additional product description: VETRINO URIGLASS + PIPETTE
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)08033673560023

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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.

W05039099DEVICES FOR SAMPLES ANALYSES - OTHER

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

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.