55 results
·
41ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
PUREWICK PATIENT TUBING
FDA Adverse Event
Malfunction
·PUREWICK CORPORATION ¿ 3012224959·Product code NZU·June 26, 2018
PUREWICK FEMALE EXTERNAL
FDA Adverse Event
Malfunction
·PUREWICK CORPORATION ¿ 3012224959·Product code NZU·August 6, 2018
PUREWICK DRYDOC STATION
FDA Adverse Event
Malfunction
·PUREWICK CORPORATION ¿ 3012224959·Product code NZU·July 30, 2018
PUREWICK FEMALE EXTERNAL CATHETER
FDA Adverse Event
Malfunction
·PUREWICK CORPORATION ¿ 3012224959·Product code NNW·October 26, 2017
PUREWICK FEMALE EXTERNAL.
FDA Adverse Event
Injury
·PUREWICK CORPORATION ¿ 3012224959·Product code NZU·November 11, 2018
PUREWICK FEMALE EXTERNAL CATHETER
FDA Adverse Event
Injury
·PUREWICK CORPORATION ¿ 3012224959·Product code NZU·December 5, 2018
PUREWICK FEMALE EXTERNAL
FDA Adverse Event
Injury
·PUREWICK CORPORATION ¿ 3012224959·Product code NZU·October 3, 2018
PUREWICK FEMALE EXTERNAL.
FDA Adverse Event
Malfunction
·PUREWICK CORPORATION ¿ 3012224959·Product code NZU·November 29, 2018
PUREWICK FEMALE EXTERNAL.
FDA Adverse Event
Injury
·PUREWICK CORPORATION ¿ 3012224959·Product code NZU·November 20, 2018
PUREWICK FEMALE EXTERNAL
FDA Adverse Event
Injury
·PUREWICK CORPORATION ¿ 3012224959·Product code NZU·October 3, 2018
PUREWICK FEMALE EXTERNAL
FDA Adverse Event
Malfunction
·PUREWICK CORPORATION ¿ 3012224959·Product code NZU·December 26, 2018
PUREWICK FEMALE EXTERNAL.
FDA Adverse Event
Injury
·PUREWICK CORPORATION ¿ 3012224959·Product code NZU·October 1, 2018
PUREWICK FEMALE EXTERNAL
FDA Adverse Event
Injury
·PUREWICK CORPORATION ¿ 3012224959·Product code NZU·May 9, 2019
PUREWICK DRY DOC STATION
FDA Adverse Event
Malfunction
·PUREWICK CORPORATION ¿ 3012224959·Product code NZU·April 8, 2019
PUREWICK FEMALE EXTERNAL CATHETER
FDA Adverse Event
Injury
·PUREWICK CORPORATION ¿ 3012224959·Product code NZU·May 2, 2019
PUREWICK FEMALE EXTERNAL
FDA Adverse Event
Injury
·PUREWICK CORPORATION ¿ 3012224959·Product code NZU·May 8, 2019
PUREWICK FEMALE EXTERNAL CATHETER
FDA Adverse Event
Injury
·PUREWICK CORPORATION ¿ 3012224959·Product code NZU·June 11, 2019
PUREWICK FEMALE EXTERNAL CATHETER
FDA Adverse Event
Injury
·PUREWICK CORPORATION ¿ 3012224959·Product code NZU·June 19, 2019
PUREWICK FEMALE EXTERNAL
FDA Adverse Event
Injury
·PUREWICK CORPORATION ¿ 3012224959·Product code NZU·April 29, 2019
PUREWICK FEMALE EXTERNAL
FDA Adverse Event
Malfunction
·PUREWICK CORPORATION ¿ 3012224959·Product code NZU·May 30, 2019