549994

Trade name

not provided

UDI-DI code

08056450501040

Basic UDI-DI

805645050MEDIAPLATES054MK

Reference / catalog number

549994

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

https://www.biolifeitaliana.it/

Clinical sizes

No clinical sizes registered for this device.

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

• W0104030299PREPARED MEDIA IN PLATES - OTHER

2 warnings 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 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.
• CW030

  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

No certificate specifically references this device's Basic UDI-DI.