5116702

Organization name

Biolife Italiana s.r.l.

SRN

IT-MF-000018174

Manufacturer status

Active

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

• CW010

  This product is a qualitative in vitro diagnostic, for professional use only; it is to be used by adequately trained and qualified laboratory personnel, observing approved biohazard precautions and aseptic techniques
• CW007

  Fragile, handle with care
• 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 the product doesn’t contain any transmissible pathogen. Therefore, it is recommended that the product 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.

Primary placement in Italy; available across 1 country total.

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

Trade name

not provided

UDI-DI code

08054187137419

Basic UDI-DI

805418713MEDIAFLASK0051E4

Reference / catalog number

5116702

Issuing entity

GS1

Risk category

IVDR Class A

Applicable legislation

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]

Status

On the market

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.

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

• W0104010306CULTURE MEDIA IN BOTTLES