COVID19/FluA+B/RSV+Radv/hMPV+hRV/PIV/M.p Ag Rapid Test P2089
COVID19/FluA+B/RSV+Radv/hMPV+hRV/PIV/M.p Ag Rapid Test P2089
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  • COVID19/FluA+B/RSV+Radv/hMPV+hRV/PIV/M.p Ag Rapid Test P2089
  • COVID19/FluA+B/RSV+Radv/hMPV+hRV/PIV/M.p Ag Rapid Test P2089

COVID19/FluA+B/RSV+Radv/hMPV+hRV/PIV/M.p Ag Rapid Test P2089

The GenSure COVID‑19/Flu A+B/RSV+Radv/hMPV+hRV /PIV/M.p Ag Rapid Test is a chromatographic immunoassay for the qualitative detection of antigen of SARS‑CoV‑2, Influenza A and Influenza B virus, Respiratory Syncytial Virus (RSV), Respiratory adenovirus (Radv), human Metapneumovirus (hMPV), human Rhinovirus (hRV), Mycoplasma pneumoniae (M.p), and Parainfluenza Viruses (PIV1+PIV2+PIV3) in nasopharyngeal swab specimens collected from individuals, who are suspected of respiratory viral or mycoplasma infection for SARS‑CoV‑2, Flu A, Flu B, RSV, Radv, hMPV, hRV, M.p and PIVs. This test is intended for use as an aid in the differential diagnosis of SARS‑CoV‑2, influenza A/B, RSV, Radv, hMPV, hRV, M.p and PIVs infections in humans in conjunction with clinical and epidemiological risk factors. It is intended for in vitro diagnostic use and professional use.

Classification: Respiratory Tract Infection


Product Description


 

 

Product Image

 

 

 

Product Specification

 

Product Name

GenSure™COVID19/FluA+B/RSV+Radv/hMPV+hRV/PIV/M.p Ag Rapid Test

Results Reading Time

15 minutes

REF

P2089

Instrument

No

Intended Use

COVID19/FluA+B/RSV+Radv/hMPV+hRV/PIV/M.p

Storage Temperature

4-30°C

Specimen type

Nasopharyngeal Swab

Shelf Life

24 months

Pack

20 pack

Certificate

CE/TFDA

 

 

 

IFU

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