2,153 results · 25ms · Sources: EU EUDAMED, US FDA

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EVIS LUCERA SMALL INTESTINAL VIDEOSCOPE

FDA Adverse Event
Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDA·June 21, 2022

EVIS LUCERA GASTROINTESTINAL VIDEOSCOPE

FDA Adverse Event
Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDS·June 21, 2022

BALLOON CONTROL UNIT

FDA Adverse Event
Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDA·June 21, 2022

SINGLE USE SPLINTING TUBE

FDA Adverse Event
Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FED·June 21, 2022

DISPOSABLE DISTAL ATTACHMENT

FDA Adverse Event
Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDS·June 21, 2022

LIGHTMAT

FDA Adverse Event
Malfunction ·LUMITEX, INC.·Product code HJN·May 19, 2010

WEE SIGHT

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code HJN·October 22, 2018

ASTODIA

FDA Adverse Event
Injury ·STIHLER ELECTRONIC, GMBH·Product code HJN·March 25, 2013

LUMITEXMD LIGHT MAT

FDA Adverse Event
Other ·LUMITEX·Product code HJN·December 31, 2009

VENOSCOPE II

FDA Adverse Event
VENOSCOPE·Product code HJN·May 4, 2005

ASTODIA

FDA Adverse Event
Injury ·STIHLER ELECTRONIC GMBH·Product code HJN·December 8, 2025

ASTODIA

FDA Adverse Event
Injury ·STIHLER ELECTRONIC GMBH·Product code HJN·December 10, 2025

TRANSILLUMINATOR

FDA Adverse Event
Injury ·STIHLER ELECTRONIC GMBH·Product code HJN·August 14, 2023

ASTODIA

FDA Adverse Event
Injury ·STIHLER ELECTRONIC GMBH·Product code HJN·December 8, 2025

VENOSCOPE TRANSILLUMINATOR

FDA Adverse Event
Injury ·VENOSCOPE, LLC·Product code HJN·May 28, 2020

VENOSCOPE II NEONATAL TRANSILLUMINATOR

FDA Adverse Event
Injury ·VENOSCOPE, LLC·Product code HJN·November 10, 2005

VENOSCOPE II NEONATAL TRANSILLUMINATOR

FDA Adverse Event
Malfunction ·VENOSCOPE, LLC·Product code HJN·November 23, 2005

ASTODIA (CONTROL UNIT)

FDA Adverse Event
Injury ·STIHLER ELECTRONIC GMBH·Product code HJN·January 30, 2024

LIGHTMAT SURGICAL ILLUMINATOR

FDA Adverse Event
Other ·LUMITEXMD, INC.·Product code HJN·November 20, 2012

VENOSCOPE

FDA Adverse Event
Product code HJN·December 7, 2016