24 results · 31ms · Sources: EU EUDAMED, US FDA

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ACMI DUR-DIGITAL URETEROSCOPE AND CHOLEDOCHOSCOPE SYSTEM

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

BELLEGLASS HP OPACEOUS DENTIN

FDA 510(k)
FDA Class 2 ·Dental

PROCERA ALLCERAM BRIDGE MATERIAL

FDA 510(k)
FDA Class 2 ·Dental

TRIAGE PROFILER SOB PANEL 25T

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code DAP·July 19, 2017

TRIAGE PROFILER SOB PANEL

FDA Adverse Event
Injury ·QUIDEL CARDIOVASCULAR INC.·Product code DAP·December 13, 2019

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FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code JHX·August 29, 2017

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FDA Adverse Event
Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code GHH·March 4, 2021

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FDA Adverse Event
Malfunction ·QUIDEL CARDIOVASCULAR, INC.·Product code DAP·August 3, 2018

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FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code DAP·January 25, 2017

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FDA Adverse Event
Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·October 23, 2019

NATURAL KNEE FLEX PROLONG ARTICULAR SURFACE

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code JWH·April 11, 2013

COSGROVE-EDWARDS ANNULOPLASTY SYSTEM

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code KRH·June 10, 2008

XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

FDA Adverse Event
Malfunction ·AV-TEMECULA-CT·Product code NIQ·April 15, 2011

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FDA Adverse Event
Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·October 5, 2018

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FDA Adverse Event
Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·January 14, 2021

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FDA Adverse Event
Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·October 31, 2019

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FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code DAP·February 10, 2017

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FDA Adverse Event
Injury ·QUIDEL CARDIOVASCULAR, INC.·Product code DAP·August 27, 2018

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FDA Adverse Event
Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code DAP·December 6, 2019

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FDA Adverse Event
Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·March 26, 2019