602 results
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117ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
PENTAX
FDA Adverse Event
Injury
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·August 11, 2017
PENTAX
FDA Adverse Event
Injury
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·August 11, 2017
PENTAX
FDA Adverse Event
HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·December 15, 2015
PENTAX
FDA Adverse Event
HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·December 15, 2015
PENTAX
FDA Adverse Event
HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·December 15, 2015
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·June 5, 2019
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·March 28, 2018
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·September 13, 2019
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·March 28, 2018
PENTAX
FDA Adverse Event
HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·December 15, 2015
PENTAX
FDA Adverse Event
HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·December 15, 2015
PENTAX
FDA Adverse Event
HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·December 15, 2015
PENTAX
FDA Adverse Event
HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·December 15, 2015
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·September 20, 2019
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·September 20, 2019
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·September 20, 2019
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·September 20, 2019
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·August 30, 2019
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·September 6, 2019
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·September 20, 2019