904 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HUMPHREY FIELD ANALYZER (HFA II)
FDA 510(k)
FDA Class 1
·Ophthalmic
FOFO
FDA UDI
Foshan Hongfeng Co., Ltd.·06971066429767·
FOFO
FDA UDI
Foshan Hongfeng Co., Ltd.·06971066422232·
FOFO
FDA UDI
Foshan Hongfeng Co., Ltd.·06971066424687·
FOFO
FDA UDI
Foshan Hongfeng Co., Ltd.·06971066423246·
GUTTA PERCHA
FDA Adverse Event
Injury
·UNK·Product code EKM·October 23, 1998
AIR-FLOW
FDA UDI
E.M.S. Electro Medical Systems S.A.·07613353202262·AIR-FLOW® handy 3.0 PERIO / PLUS Premium
Adapte...
hailie - For use only with Serevent HFA
FDA UDI
ADHERIUM (NZ) LIMITED·09421032180231·Non-rechargeable Battery
PROVENTIL HFA
FDA Adverse Event
Malfunction
·SCHERING-PLOUGH·Product code CCQ·July 7, 2011
PROAIR HFA
FDA Adverse Event
IVAX PHARMACY, IRELAND, IVAX LAB·Product code CAF·January 23, 2007
PROAIR HFA
FDA Adverse Event
Injury
·IVAX PHARMACEUTICAL / TEVA PHARMACEUTICAL·Product code KCO·August 30, 2018
PROAIR HFA
FDA Adverse Event
Injury
·TEVA RESPIRATORY, LLC·Product code CAF·November 25, 2016
PROAIR (HFA)
FDA Adverse Event
UNK·Product code CCQ·July 2, 2007
PROAIR HFA
FDA Adverse Event
Malfunction
·IVA/TEVA·Product code CCQ·September 5, 2012
PROAIR HFA
FDA Adverse Event
Malfunction
·TEVA RESPIRATORY LLC·Product code CAF·August 22, 2013
PROAIR HFA
FDA Adverse Event
Injury
·TEVA PHARMACEUTICALS USA·Product code CAF·February 20, 2018
PROAIR HFA
FDA Adverse Event
Injury
·TEVA PHARMACEUTICAL·Product code KCO·January 5, 2018
Hailie Sensor - for use only with Flovent HFA
FDA UDI
ADHERIUM (NZ) LIMITED·09421032180200·Non-rechargeable battery
Hailie Sensor - for use only with Flovent HFA
FDA UDI
ADHERIUM (NZ) LIMITED·09421032180101·Rechargeable battery
Hailie Sensor - for use only with ProAir HFA
FDA UDI
ADHERIUM (NZ) LIMITED·09421032180163·Rechargeable battery