155 results · 39ms · Sources: EU EUDAMED, US FDA

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ACCU-CHEK ULTRAFLEX INFUSION SET

FDA Adverse Event
Injury ·ROCHE INSULIN DELIVERY SYSTEMS, INC.·Product code FPA·January 12, 2012

ACCU-CHEK SPIRIT

FDA Adverse Event
Injury ·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·January 12, 2012

BIOROOT RCS

FDA Adverse Event
Injury ·SEPTODONT, INC.·Product code KIF·October 23, 2017

BIOROOT RCS

FDA Adverse Event
Injury ·SEPTODONT SAS·Product code KIF·August 28, 2023

BIOROOT RCS

FDA Adverse Event
Injury ·SEPTODONT, INC.·Product code KIF·July 4, 2017

PATIENT INFORMATION CENTER IX

FDA Adverse Event
Injury ·PHILIPS NORTH AMERICA LLC·Product code MHX·June 6, 2022

NV MICROCATHETER

FDA Adverse Event
Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·November 10, 2023

CAIRE STROLLER PORTABLE

FDA Adverse Event
Injury ·CAIRE, INC.·Product code BYJ·April 13, 2010

PATIENT INFORMATION CENTER IX

FDA Adverse Event
Injury ·PHILIPS NORTH AMERICA LLC·Product code MHX·December 27, 2021

OLYMPUS RC+S

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·July 20, 2021

SUMMIT RC+S

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·October 1, 2024

NUCLEUS 24 RCS

FDA Adverse Event
Injury ·COCHLEAR LTD.·Product code MCM·May 7, 2004

NUCLEUS CI24 RCS

FDA Adverse Event
Injury ·COCHLEAR LTD·Product code MCM·May 7, 2004

SUMMIT RC+S

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·October 17, 2023

THERMOCOOL® SF NAV UNI-DIRECTIONAL CATHETER

FDA Adverse Event
Injury ·BIOSENSE WEBSTER INC·Product code LPB·August 29, 2024

COAGUCHECK XS

FDA Adverse Event
Injury ·ROCHE DIAGNOSTICS GMBH·Product code GJS·December 4, 2024

COAGUCHECK XS

FDA Adverse Event
Injury ·ROCHE DIAGNOSTICS GMBH·Product code GJS·December 4, 2024

COAGUCHECK XS

FDA Adverse Event
Injury ·ROCHE DIAGNOSTICS GMBH·Product code GJS·December 4, 2024

PATIENT INFORMATION CENTER IX

FDA Adverse Event
Injury ·PHILIPS MEDICAL SYSTEMS·Product code MHX·August 8, 2023

ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM

FDA Adverse Event
Injury ·CORDIS NEUROVASCULAR, INC.·Product code NJE·November 1, 2011