Service Hotline: +86 4006196063
NMPA Registration Certificate:
GXZZ 20153401899
Sample Type:
Swab Specimen
Pack Size:
32 tests/kit
Intended Use:
The product is used for the in vitro qualitative detection of mycoplasma pneumoniae nucleic acid in human oropharyngeal swab specimens
Limit of detection:1000 CCU/mL
The coincidence rates of both positive and negative references can reach 100%.
The coefficient of variation (CV) of Ct value of precision reference standard is below 5%, which fully meets the requirements of industry standards.
UNG enzyme and dUTP are used to effectively prevent the contamination of amplified products to avoid false positive results