617 results
·
42ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
PRESIDIO 18 - CERECYTE MICROCOIL
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SARL·Product code HCG·October 25, 2017
DELTAPAQ - CERECYTE MICROCOIL
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SARL·Product code HCG·October 31, 2017
DELTAPL CERE COIL 10 SYS 2X3
FDA Adverse Event
Malfunction
·REFER TO SECTION H10·Product code HCG·April 23, 2018
UNKNOWN
FDA Adverse Event
Malfunction
·COOK INC·Product code KRD·November 13, 2019
UNKNOWN
FDA Adverse Event
Malfunction
·COOK INC·Product code KRD·November 13, 2019
UNKNOWN
FDA Adverse Event
Malfunction
·COOK INC·Product code KRD·November 13, 2019
UNKNOWN
FDA Adverse Event
Malfunction
·COOK INC·Product code KRD·November 13, 2019
UNKNOWN
FDA Adverse Event
Malfunction
·COOK INC·Product code KRD·November 13, 2019
UNKNOWN
FDA Adverse Event
Malfunction
·COOK INC·Product code KRD·November 13, 2019
DELTAPAQ CERE 3MMX6CM
FDA Adverse Event
Malfunction
·Product code HCG·March 15, 2018
DELTAXTRASOFT COIL
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SARL·Product code HCG·November 28, 2017
DELTAFILL18 14MM X 45CM
FDA Adverse Event
Malfunction
·SEE H.10·Product code KRD·August 28, 2018
DELTAPLUSH - PLATINUM MICROCOIL
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SARL·Product code HCG·December 7, 2017
MICRUSFRAME COIL
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SARL·Product code HCG·December 20, 2017
PRESIDIO 10 - CERECYTE MICROCOIL
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SARL·Product code HCG·January 3, 2018
DELTAPAQ - CERECYTE MICROCOIL
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SARL·Product code HCG·October 17, 2017
ULTIPAQ - PLATINUM MICROCOIL
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SARL·Product code HCG·October 13, 2017
MSPHERE 10 CERE, 5MMX9.7CM
FDA Adverse Event
Malfunction
·REFER TO SECTION H10·Product code HCG·January 14, 2019
DELTAPAQ 2.5MMX8CM SR PLAT
FDA Adverse Event
Malfunction
·SEE H.10·Product code KRD·July 23, 2018
COIL-THERMO MECHANICAL
FDA Adverse Event
Malfunction
·SEE H.10·Product code KRD·January 29, 2019