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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

5118102 — IVDR Class A IVDR by Mascia Brunelli S.p.A.

MD Atlas
Mascia Brunelli S.p.A.

EUDAMED last updated this device on May 29, 2026

5118102

8055594457268MEDIAFLASKQA

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Mascia Brunelli S.p.A.
UDI-DI code: 08055594457503
Reference / catalog number: 5118102

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View device family (Basic UDI)

Manufacturer information

Organization name: Mascia Brunelli S.p.A.
SRN: IT-MF-000009572
Manufacturer status: Active

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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.

Critical warnings

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

CW267
This culture medium contains raw materials of animal origin. The ante and post mortem controls of the animals and those during the production and distribution cycle of the raw materials, cannot completely guarantee that these products do not contain any transmissible pathogen. Therefore, it is recommended that the ready-to-use tubes be treated as potentially infectious, and handled observing the usual specific precautions: do not ingest, inhale, or allow to come into contact with skin, eyes, mucous membranes. Download the TSE Statement from the website www.biolifeitaliana.it, describing the measures implemented by Biolife Italiana for the risk reduction linked to infectious animal diseases.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement	Oct 1, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08055594457503
Basic UDI-DI: 8055594457268MEDIAFLASKQA
Reference / catalog number: 5118102
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: —
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
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Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08055594457503

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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.

W0104010306CULTURE MEDIA IN BOTTLES

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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