73 results · 19ms · Sources: EU EUDAMED, US FDA

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COR17000868-000

FDA Adverse Event
No answer provided ·Product code RCC·November 9, 2017

COR17000835-000

FDA Adverse Event
No answer provided ·Product code RCC·October 25, 2017

COR17000964-000

FDA Adverse Event
No answer provided ·Product code RCC·December 19, 2017

COR17000835-001

FDA Adverse Event
No answer provided ·Product code RCC·November 30, 2017

COR17000901-001

FDA Adverse Event
No answer provided ·Product code RCC·December 22, 2017

COR17000955-000

FDA Adverse Event
No answer provided ·Product code RCC·December 14, 2017

COR17000867-000

FDA Adverse Event
No answer provided ·Product code RCC·November 9, 2017

COR17000901-000

FDA Adverse Event
No answer provided ·Product code RCC·November 21, 2017

COR17000867-001

FDA Adverse Event
No answer provided ·Product code RCC·December 11, 2017

COR17000868-001

FDA Adverse Event
No answer provided ·Product code RCC·December 22, 2017

COR18001302-000

FDA Adverse Event
No answer provided ·Product code RCC·July 30, 2018

COR18001301-000

FDA Adverse Event
No answer provided ·Product code RCC·July 30, 2018

COR18001042-001

FDA Adverse Event
No answer provided ·Product code RCC·August 10, 2018

COR18001044-001

FDA Adverse Event
No answer provided ·Product code RCC·August 10, 2018

COR18001176-001

FDA Adverse Event
No answer provided ·Product code RCC·August 10, 2018

COR18001262-000

FDA Adverse Event
No answer provided ·Product code RCC·July 20, 2018

COR18000919-001

FDA Adverse Event
No answer provided ·Product code RCC·July 30, 2018

COR18001175-001

FDA Adverse Event
No answer provided ·Product code RCC·August 10, 2018

COR18001349-000

FDA Adverse Event
No answer provided ·Product code RCC·August 10, 2018

COR18001129-001

FDA Adverse Event
No answer provided ·Product code RCC·August 10, 2018