12 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
D901 LILLIPUT OXYGENATOR
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA·Product code DTZ·October 13, 2021
PROLIFT PELVIC FLOOR REPAIR
FDA Adverse Event
Injury
·ETHICON INC·Product code OTP·February 10, 2013
ENDOTAK RELIANCE
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code LWS·July 23, 2014
CONTAK RENEWAL
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·January 10, 2011
CER BIOLOXD OPTION HD 40MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·June 26, 2019
CUSTOM PERFUSION PACK
FDA Adverse Event
Other
·SORIN GROUP ITALIA·Product code DTZ·October 30, 2012
BIOLOX DELTA CER OPTION HD 36MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·July 14, 2025
LILLIPUT 1 START
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA SRL·Product code DTZ·April 17, 2023
LILLIPUT 1 OXYGENATOR
FDA Adverse Event
Malfunction
·SORIN GROUP ITALY·Product code DTZ·December 27, 2024
LILLIPUT 1 NEW BORN HOLLOW FIBER OXYGENATOR
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA·Product code DTZ·December 6, 2024
LILLIPUT 1 NEW BORN HOLLOW FIBER OXYGENATOR
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA SRL·Product code DTZ·January 17, 2022
LILLIPUT 1 NEW BORN HOLLOW FIBER OXYGENATOR
FDA Adverse Event
Malfunction
·SORIN GROUP ITALIA SRL·Product code DTZ·January 25, 2022