6,454 results
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49ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SERF 90-ASD PROBE
FDA Adverse Event
Malfunction
·STRYKER ENDOSCOPY PUERTO RICO·Product code GEI·July 14, 2005
EVIS EXERA II XENON LIGHT SOURCE
FDA Adverse Event
Malfunction
·SHIRAKAWA OLYMPUS CO., LTD.·Product code NWB·May 1, 2024
EVIS EXERA III COLONOVIDEOSCOPE
FDA Adverse Event
Malfunction
·AIZU OLYMPUS CO., LTD.·Product code FDF·May 23, 2026
GASTROINTESTINAL VIDEOSCOPE
FDA Adverse Event
Malfunction
·AIZU OLYMPUS CO., LTD.·Product code FDS·December 10, 2025
ENDOEYE FLEX DEFLECTABLE VIDEOSCOPE
FDA Adverse Event
Malfunction
·OLYMPUS MEDICAL SYSTEMS CORP.·Product code GCJ·December 24, 2020
EAGLE STERILIZER
FDA Adverse Event
STERIS MEXICO, S. DE R.L. DE C.V.·Product code FLE·May 18, 2011
DORNIER HOLMIUM LASER FIBER
FDA Adverse Event
Malfunction
·DORNIER MEDTECH AMERICA, INC.·Product code GEX·October 6, 2016
LCS 3PEG MOD ROT PAT CEM STD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code HTG·December 21, 2005
X-7000 LIGHTSOURCE
FDA Adverse Event
Malfunction
·STRYKER ENDOSCOPY·Product code FFS·March 2, 2006
COLONOVIDEOSCOPE
FDA Adverse Event
Malfunction
·AIZU OLYMPUS CO., LTD.·Product code FDF·October 27, 2025
EVIS LUCERA ULTRASONIC BRONCHOFIBERVIDEOSCOPE
FDA Adverse Event
Malfunction
·SHIRAKAWA OLYMPUS CO., LTD.·Product code PSV·October 23, 2024
EVIS LUCERA ULTRASONIC BRONCHOFIBERVIDEOSCOPE
FDA Adverse Event
Malfunction
·SHIRAKAWA OLYMPUS CO., LTD.·Product code PSV·October 23, 2024
EVIS EXERA III BRONCHOVIDEOSCOPE
FDA Adverse Event
Malfunction
·AIZU OLYMPUS CO., LTD.·Product code EOQ·November 27, 2024
EVIS LUCERA ULTRASONIC BRONCHOFIBERVIDEOSCOPE
FDA Adverse Event
Malfunction
·SHIRAKAWA OLYMPUS CO., LTD.·Product code PSV·October 23, 2024
EVIS LUCERA ULTRASONIC BRONCHOFIBERVIDEOSCOPE
FDA Adverse Event
Malfunction
·SHIRAKAWA OLYMPUS CO., LTD.·Product code PSV·October 23, 2024
EVIS LUCERA ULTRASONIC BRONCHOFIBERVIDEOSCOPE
FDA Adverse Event
Malfunction
·SHIRAKAWA OLYMPUS CO., LTD.·Product code PSV·October 23, 2024
EVIS EXERA III BRONCHOVIDEOSCOPE
FDA Adverse Event
Malfunction
·AIZU OLYMPUS CO., LTD.·Product code EOQ·January 3, 2025
RAPICIDE HIGH LEVEL DISINFECTANT
FDA Adverse Event
MEDIVATORS·Product code MED·May 7, 2015
PKG L9000 LIGHT SOURCE
FDA Adverse Event
Malfunction
·STRYKER ENDOSCOPY-SAN JOSE·Product code FCW·August 26, 2019
X6000 XENON LIGHTSOURCE
FDA Adverse Event
Injury
·STRYKER ENDOSCOPY·Product code GCT·July 1, 2002