8 results
·
50ms
·
Sources: EU EUDAMED, US FDA
MC-500
FDA Adverse Event
Malfunction
·NIDEK CO. LTD.·Product code HQF·March 1, 2019
BLADDERSCAN
FDA Adverse Event
Injury
·DIAGNOSTIC ULTRASOUND INC.·Product code ITX·October 23, 2003
MC-500
FDA Adverse Event
Malfunction
·NIDEK INCORPORATED·Product code HQF·January 9, 2017
O-ARM 1000 IMAGING SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC. (LITTLETON)·Product code OXO·November 14, 2016
O-ARM 1000 IMAGING SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC. (LITTLETON)·Product code OXO·November 7, 2016
O-ARM 1000 IMAGING SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC. (LITTLETON)·Product code OXO·August 3, 2016
WEBSTER CS CATHETER WITH AUTO ID TECHNOLOGY
FDA Adverse Event
Death
·BIOSENSE WEBSTER INC·Product code DRF·June 26, 2024
Emergo Europe B.V.
Authorized representative
🇳🇱 Netherlands·900 Manufacturers·22100 Devices