18 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
MReye Embolization Coils
FDA 510(k)
FDA Class 2
·Cardiovascular
MREYE EMBOLIZATION COIL
FDA Adverse Event
Injury
·COOK INC·Product code KRD·May 11, 2018
MREYE EMBOLIZATION COIL
FDA Adverse Event
Injury
·COOK INC·Product code KRD·May 11, 2018
MREYE EMBOLIZATION COIL
FDA Adverse Event
Injury
·COOK INC·Product code KRD·May 11, 2018
NESTER PLATINUM EMBOLIZATION MICROCOIL
FDA Adverse Event
Injury
·COOK INC·Product code KRD·May 11, 2018
MREYE EMBOLIZATION COIL
FDA Adverse Event
Injury
·COOK INC·Product code KRD·May 11, 2018
MREYE EMBOLIZATION COIL
FDA Adverse Event
Injury
·COOK INC·Product code KRD·May 11, 2018
STAINLESS STEEL EMBOLIZATION COIL
FDA Adverse Event
Malfunction
·COOK INC·Product code KRD·August 24, 2017
Oticon
FDA UDI
Oticon A/S·05707131284181·RIA2 PRO TI, BTE 13 WL 85 DBL
6 FR DL POWERPICC CATHETER
FDA 510(k)
FDA Class 2
·General Hospital
MYLABTWICE, MODEL 6200
FDA 510(k)
FDA Class 2
·Radiology
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 6, 2013
HIP HEAD, 10/12 TAPER, 28MM, +0MM
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWY·June 29, 2011
SOFTCLIX LANCET DEVICE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FMK·September 3, 2008
TRIFORCE¿ PERIPHERAL CROSSING SET
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·February 4, 2020
TRIFORCE¿ PERIPHERAL CROSSING SET
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·January 2, 2020
TRIFORCE¿ PERIPHERAL CROSSING SET
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·February 4, 2020
TRIFORCE¿ PERIPHERAL CROSSING SET
FDA Adverse Event
Injury
·COOK INC·Product code KRA·January 2, 2020