106 results
·
40ms
·
Sources: EU EUDAMED, US FDA
QUIDEL CORP.
FDA registration
QUIDEL CORP.·23 products·🇺🇸 United States
SOFIA FLUORESCENT IMMUNOASSAY ANALYZER
FDA Adverse Event
Malfunction
·QUIDEL CORP·Product code GNX·March 20, 2014
SOFIA FLUORESCENT IMMUNOASSAY ANALYZER
FDA Adverse Event
Malfunction
·QUIDEL CORP.·Product code GNX·March 11, 2014
SOFIA INFLUENZA A+B
FDA Adverse Event
Death
·QUIDEL CORP.·Product code GNX·August 12, 2015
SOFIA INFLUENZA A+B FIA
FDA Adverse Event
Death
·QUIDEL CORP.·Product code GNX·December 28, 2012
QUIDEL QUICKVUE AT HOME OTC COVID-19 TEST
FDA Adverse Event
Malfunction
·QUIDEL CORP.·Product code QKP·December 14, 2021
COVID 19 SWAB TEST SOFIA ANTIGEN SWAB TEST
FDA Adverse Event
Malfunction
·QUIDEL CORP.·Product code QKP·December 16, 2021
QUICKVUE COVID TEST PI ONLINE WITH FDA
FDA Adverse Event
Malfunction
·QUIDEL CORP.·Product code QKP·November 8, 2021
QUIDEL QUICKVUE AT-HOME OTC COVID-19 TEST
FDA Adverse Event
Malfunction
·QUIDEL CORP.·Product code QKP·November 12, 2021
QUICKVUE AT-HOME OTC COVID-19 TEST
FDA Adverse Event
Malfunction
·QUIDEL CORP.·Product code QKP·December 16, 2021
QUICKVUE AT-HOME OTC COVID-19 TEST
FDA Adverse Event
Malfunction
·QUIDEL CORP.·Product code QKP·October 21, 2021
QUICKVUE
FDA Adverse Event
Malfunction
·QUIDEL CORP.·Product code QKP·October 21, 2021
CARDS Q.S., HCG SERUM/URINE
FDA Adverse Event
Other
·QUIDEL CORP·Product code JHI·February 27, 2002
OVU-QUICK ONE-STEP
FDA Adverse Event
Malfunction
·QUIDEL CORP·Product code NGE·October 20, 2003
OUICKVUE+ RAPID STREP A TEST
FDA Adverse Event
Malfunction
·QUIDEL CORP·Product code GTY·December 10, 2003
QUIDEL QUICKVUE ONE STEP
FDA Adverse Event
Malfunction
·QUIDEL CORP.·Product code JHJ·September 25, 2000
QUIDEL QUIK-VUE HCG COMBO
FDA Adverse Event
Malfunction
·QUIDEL CORP.·Product code JHJ·June 2, 2000
SOFIA INFLUENZA A AND B FIA KIT
FDA Adverse Event
Other
·QUIDEL CORP·Product code GNX·December 11, 2012
QUIDEL STREP A TEST
FDA Adverse Event
Malfunction
·QUIDEL CORP.·Product code GTZ·January 29, 2013
QUIDEL
FDA Adverse Event
Malfunction
·QUIDEL CORP.·Product code JHJ·January 23, 2003