Decheng 2019-nCoV AgSalivaRapid Test Card

Certificate verification page

Certification scheme

98/79/EC Annex III section 6

Certificate number

IVDD 21 042 0106

Certificate history

IVDD 21 042 0106 (Initial issue |26.Nov.2021)

Manufacturer/Holder of certificate

Guangzhou Decheng Biotechnology Co., Ltd

Room 218 and Room 212, Building 2, No. 68, Nanxiang 1st Road, Science City, Huangpu District, Guangzhou, Guangdong, 510663, P.R. China

Other sites
Effective from

26.Nov.2021

Valid until

26.May.2022

Suspension period
Withdrawn on
Validity status
Valid
Validity conditions

The manufacturer has a duty to submit to the Notified body testing results as per established procedure of each manufactured batch prior its releasing.

Products within scope

2019-nCoV AgSalivaRapid Test Card (Immunochromatography)

 

2019-nCoV Ag Saliva Rapid Test Card is an antigen rapid test on basis of lateral flow immunochromatographic assay intended for the rapid and qualitative detection of N-antigen of human coronavirus 2 (2019-nCoV) in saliva samples from individuals suspected of COVID-19.

 

Types/Categories/Models:
1 test per box, 5 tests per box, 20 tests per box (0699C8X001, 0699C8X005, 0699C8X020)
Classification

Devices for self-testing