19 results · 23ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

PIPELINE

FDA Adverse Event
Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·February 8, 2022

ENDURANT

FDA Adverse Event
Death ·MEDTRONIC IRELAND·Product code MIH·November 4, 2014

KAYSERBETT OLAF

FDA Adverse Event
Death ·KAYSERBETTEN GMBH & CO. KG·Product code FNL·April 23, 2026

ECHELON

FDA Adverse Event
Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·September 11, 2025

EVIS LUCERA ELITE SMALL INTESTINALVIDEOSCOPE

FDA Adverse Event
Death ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDA·October 31, 2018

BALLOON CONTROL UNIT

FDA Adverse Event
Death ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDA·July 7, 2020

UNK

FDA Adverse Event
Death ·UNK·Product code HDA·January 19, 2007

FUJIFILM DOUBLE BALLOON ENDOSCOPE EN-450T5

FDA Adverse Event
Death ·FUJIFILM CORPORATION·Product code FDA·August 7, 2023

FUJIFILM DOUBLE BALLOON ENDOSCOPE EN-450T5

FDA Adverse Event
Death ·FUJIFILM CORPORATION·Product code FDA·August 11, 2023

FUJIFILM DOUBLE BALLOON ENDOSCOPE, EN-450T5, EN450P5

FDA Adverse Event
Death ·FUJIFILM CORPORATION·Product code FDA·September 22, 2023

EVIS EXERA II SMALL INTESTINAL VIDEOSCOPE

FDA Adverse Event
Death ·AIZU OLYMPUS CO., LTD.·Product code FDA·January 2, 2024

FUJIFILM DOUBLE BALLOON ENDOSCOPES EN-450T5/W

FDA Adverse Event
Death ·FUJIFILM CORPORATION·Product code FDA·January 26, 2024

FUJIFILM DOUBLE BALLOON ENDOSCOPE EI-580BT

FDA Adverse Event
Death ·FUJIFILM CORPORATION·Product code FDA·June 22, 2023

TUCKER-MCLEAN FORCEPS

FDA Adverse Event
Death ·V. MUELLER DIV. BAXTER HEALTHCARE CORP.·Product code HDA·June 2, 1994

TUCKER MCLEAN FORCEPS

FDA Adverse Event
Death ·PILLING SURGICAL INSTRUMENTS·Product code HDA·November 14, 1997

TUCKER MCLEAN FORCEPS

FDA Adverse Event
Death ·PILLING SURGICAL INSTRUMENTS·Product code HDA·December 15, 1997

OLYMPUS SMALL INTESTINAL VIDEOSCOPE SYSTEM

FDA Adverse Event
Death ·OLYMPUS MEDICAL SYSTEM CORP·Product code FDA·October 18, 2013

FORCEPS

FDA Adverse Event
Death ·*·Product code HDA·August 7, 2001

EVIS EXERA II SMALL INTESTINAL VIDEOSCOPE

FDA Adverse Event
Death ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDA·March 18, 2020