Note: Ingredients listed on restricted chemical lists
General Information
Revision date
2021-04-05
Product name
Rapid ResponseTM COVID-19 Antigen Rapid Test Device
Substance name
antigens from human nasopharyngeal secretions and nasal
CAS No.
26628-22-8
1.2.1 Relevant identified uses
In vitro diagnostic rapid test, it is intended to aid in the rapid
Manufacturer Name
570 Hood Road
Icons in SDS
Company Information
company name
BTNX Inc
e-mail address of the competent person responsible for the Safety Data Sheet
info@btnx.com
Section 2
CLP CLASSIFICATION
mixture The product is not classified according to the CLP regulation
2.2 Label elements
Labelling according to Regulation (EC) No 1272/2008 The product is not classified according to the CLP regulation No particular hazards if test is used according to the instructions.
2.3 Other hazards
The product contains chemicals and materials of animal origin. Although the risk of infection is rated as extremely unlikely, a direct contact should be avoided.
