4,548 results · 42ms · Sources: EU EUDAMED, US FDA

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PUMA-G SYSTEM

FDA Adverse Event
Death ·COAPTECH, INC.·Product code KGC·September 21, 2023

PUMA-G SYSTEM

FDA Adverse Event
Injury ·COAPTECH, INC.·Product code KGC·June 27, 2024

PUMA-G SYSTEM

FDA Adverse Event
Injury ·COAPTECH, INC.·Product code KGC·March 5, 2025

PGW .018 SV SHORT 180CM ST

FDA Adverse Event
Injury ·CORDIS CORPORATION·Product code DQX·January 5, 2022

PGW .018 SV SHORT 180CM ST

FDA Adverse Event
Injury ·CORDIS CORPORATION·Product code DQX·January 11, 2022

PGW .018 SV SHORT 300CM ST

FDA Adverse Event
Malfunction ·CORDIS CORPORATION·Product code DQX·September 2, 2021

HI-TORQUE WHISPER GUIDE WIRES

FDA Adverse Event
Injury ·ABBOTT VASCULAR·Product code DQX·April 4, 2023

PGW .018 SV SHORT 300CM ST

FDA Adverse Event
Malfunction ·CORDIS CORPORATION·Product code DQX·September 22, 2021

PGW .018 SV SHORT

FDA Adverse Event
Malfunction ·CORDIS CORPORATION·Product code DQX·November 20, 2008

PUMA-G SYSTEM

FDA Adverse Event
Malfunction ·COAPTECH, INC.·Product code KGC·November 30, 2023

PGW .018 SV SHORT 180CM ST

FDA Adverse Event
Malfunction ·LAKE REGION·Product code DQX·October 24, 2016

PGW

FDA Adverse Event
Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·December 10, 2018

PGW .018 SV SHORT

FDA Adverse Event
Malfunction ·CORDIS CORPORATION·Product code DQX·June 15, 2012

PGW .018 SV SHORT 300CM ST

FDA Adverse Event
Injury ·CORDIS CORPORATION·Product code DQX·June 30, 2020

PGW .018 SV SHORT 300CM ST

FDA Adverse Event
Malfunction ·CORDIS CORPORATION·Product code DQX·August 10, 2021

CORDIS REFLEX STEERABLE GUIDEWIRE

FDA Adverse Event
Malfunction ·CORDIS CORPORATION·Product code DQX·July 27, 2016

PGW .018 SV INTER 180CM ST

FDA Adverse Event
Malfunction ·CORDIS CORPORATION·Product code DQX·September 15, 2016

PGW .018 SV SHORT

FDA Adverse Event
Malfunction ·CORDIS CORPORATION·Product code DQX·March 4, 2015

PGW .018 SV SHORT 300CM ST

FDA Adverse Event
Malfunction ·CORDIS CORPORATION·Product code DQX·June 20, 2022

PUMA-G SYSTEM

FDA Adverse Event
Malfunction ·COAPTECH, INC.·Product code KGC·June 23, 2025