37 results · 32ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

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
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
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 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
Injury ·PUREWICK CORPORATION ¿ 3012224959·Product code NZU·May 9, 2019

PUREWICK FEMALE EXTERNAL

FDA Adverse Event
Injury ·PUREWICK CORPORATION ¿ 3012224959·Product code NZU·May 31, 2019

PUREWICK FEMALE EXTERNAL CATHETER

FDA Adverse Event
Injury ·PUREWICK CORPORATION ¿ 3012224959·Product code NZU·May 14, 2019

PUREWICK FEMALE EXTERNAL

FDA Adverse Event
Injury ·PUREWICK CORPORATION ¿ 3012224959·Product code NZU·July 12, 2018

PUREWICK FEMALE EXTERNAL.

FDA Adverse Event
Injury ·PUREWICK CORPORATION ¿ 3012224959·Product code NZU·July 17, 2018

PUREWICK FEMALE EXTERNAL

FDA Adverse Event
Injury ·PUREWICK CORPORATION ¿ 3012224959·Product code NZU·August 29, 2018

PUREWICK FEMALE EXTERNAL

FDA Adverse Event
Injury ·PUREWICK CORPORATION ¿ 3012224959·Product code NZU·July 25, 2018

PUREWICK FEMALE EXTERNAL CATHETER

FDA Adverse Event
Injury ·PUREWICK CORPORATION ¿ 3012224959·Product code NZU·January 23, 2019