6,454 results · 49ms · Sources: EU EUDAMED, 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