iLite IL-2 Assay Ready Cells

CLP CLASSIFICATION

The mixture is not to be classified according to CLP. The mixture is covered by Directive 2009/41/EC on the contained use of genetically modified micro-organisms and classified as a Class 1 Genetically Modified Microorganism. The mixture is covered by Directive 2000/54/EC of 18 September 2000 on the protection of workers from risks related to exposure to biological agents at work.

2.2 Label elements

None

2.3 Other hazards

Other hazards which do Contain Fetal Bovine serum, which is derived from cattle. The Certificate of Analysis for not result in FBS show that the substance has been analyzed for Bovine Adenovirus, Bovine

2.1 Classification of the substance or mixture

Parvovirus, Blue tongue Virus, Bovine Virus Diarrhea, Infectious Bovine Rhinotracheitis, Parainfluenza 3, Rabies Virus, Reovirus, Bovine Respiratory Syncytial Virus, Vesicular Stomatitis Virus, Cytopathic agents and Hemadsorbing agents with a negative result. The FBS was collected in New Zealand. The serum was not collected from cattle born, raised, shipped through or slaughtered in countries where Bovine Spongiform Encephalopathy is known to exist. The products are considered to be biological agents in group 1 (ie. a biological agent that is unlikely to cause human infection). As a precaution, it is recommended that the work is carried out under measures similar to Group 2 in Council Directive 2000/54/EC. Substance meets the criteria for PBT/ vPvB under

PBT Substances

vPvB No Regulation EC No. 1907/2006, appendix XIII