76 results · 35ms · 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.

FUJIFILM DOUBLE BALLOON ENDOSCOPE EI-580BT

FDA Adverse Event
Malfunction ·FUJIFILM CORPORATION·Product code FDA·March 6, 2023

FUJIFILM DOUBLE BALLOON ENDOSCOPE EI-580BT

FDA Adverse Event
Malfunction ·FUJIFILM CORPORATION·Product code FDA·May 18, 2022

FUJIFILM DOUBLE BALLOON ENDOSCOPE EI-580BT

FDA Adverse Event
Malfunction ·FUJIFILM CORPORATION·Product code FDA·May 18, 2022

FUJIFILM DOUBLE BALLOON ENDOSCOPE EI-580BT

FDA Adverse Event
Injury ·FUJIFILM CORPORATION·Product code FDA·March 6, 2023

FUJIFILM DOUBLE BALLOON ENDOSCOPE EI-580BT

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

FUJIFILM DOUBLE BALLOON ENDOSCOPE EI-580BT

FDA Adverse Event
Injury ·FUJIFILM CORPORATION·Product code FDA·January 5, 2023

FUJIFILM DOUBLE BALLOON ENDOSCOPE EI-580BT

FDA Adverse Event
Injury ·FUJIFILM CORPORATION·Product code FDA·January 6, 2023

FUJIFILM DOUBLE BALLOON ENDOSCOPE EI-580BT

FDA Adverse Event
Injury ·FUJIFILM CORPORATION·Product code FDA·March 13, 2023

ENDOSCOPE MODEL EI-740D/S

FDA Adverse Event
Malfunction ·FUJIFILM CORPORATION·Product code FDS·March 19, 2024

ECHELON XL MRI SYSTEM

FDA Adverse Event
Injury ·FUJIFILM CORPORATION·Product code LNH·July 30, 2025

ECHELON XL MRI SYSTEM

FDA Adverse Event
Injury ·FUJIFILM CORPORATION·Product code LNH·July 30, 2025

GELLHORN PESS.FLEX.2-1/2

FDA Adverse Event
Malfunction ·COOPERSURGICAL, INC.·Product code HHW·August 24, 2023

FUJIFILM DOUBLE BALLOON ENDOSCOPE EI-580BT

FDA Adverse Event
Injury ·FUJIFILM CORPORATION·Product code FDA·October 25, 2019

LIFEVEST WCD 4000 SYSTEM

FDA Adverse Event
Injury ·ZOLL MANUFACTURING CORPORATION·Product code MVK·December 13, 2018

LIFEVEST WCD 4000 SYSTEM

FDA Adverse Event
Injury ·ZOLL MANUFACTURING CORPORATION·Product code MVK·December 4, 2018

FUJIFILM DOUBLE BALLOON ENDOSCOPE EI-580BT

FDA Adverse Event
Injury ·FUJIFILM CORPORATION·Product code FDA·October 25, 2019

INTERJECT?

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code FCG·April 2, 2013

FUJINON

FDA Adverse Event
Injury ·FUJIFILM TECHNO PRODUCTS CO., LTD. MITO SITE·Product code FDA·June 22, 2017

santec OIS Corporation

Manufacturer
🇯🇵 Japan

santec OIS Corporation

FDA registration
santec OIS Corporation·2 products·🇯🇵 Japan