26 results
·
31ms
·
Sources: EU EUDAMED, US FDA
MODIFICATION TO ALARMVIEW WIRELESS DATA NETWORK SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
Dornier MedTech
FDA UDI
DORNIER MEDTECH AMERICA, INC.·04049958003127·400 micron Holmium Laser Fiber Cable, Single Us...
SASSY JONES
FDA UDI
FGX INTERNATIONAL INC.·00193033464908·
SASSY JONES
FDA UDI
FGX INTERNATIONAL INC.·00193033464885·
SASSY JONES
FDA UDI
FGX INTERNATIONAL INC.·00193033464915·
SASSY JONES
FDA UDI
FGX INTERNATIONAL INC.·00193033464922·
SASSY JONES
FDA UDI
FGX INTERNATIONAL INC.·00193033464878·
SASSY JONES
FDA UDI
FGX INTERNATIONAL INC.·00193033464892·
MALE LUER SLIP 64 CAV.
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·March 19, 2021
MALE LUER SLIP 64 CAV.
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FPA·April 9, 2021
BLASTASSIST SYSTEM
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
SLEEP PAT 200 DEVICE
FDA 510(k)
FDA Class 2
·Anesthesiology
MALE LUER ADAPTOR
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FPA·May 13, 2021
ACRYSOF
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·September 13, 2013
ACRYSOF
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·September 13, 2013
NC Traveler RX Coronary Dilatation Catheter, Part No. 1013152-12, 1013152-15, 1013152-20, 1013153-08, 1013153-12, 1013153-15, 1013153-20, 1013154-08, 1013154-12, 1013154-15, 1013154-20, 1013155-08, 1013155-12 1013155-15, 1013155-20, 1013156-12, 1013156-15, 1013157-08, 1013157-12, 1013157-15
FDA Enforcement
Class I
·Terminated·Abbott Vascular·May 24, 2017
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS·Product code JAA·March 1, 2013
ASR ACETABULAR IMPLANT 50
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·February 24, 2011
CARPENTIER-EDWARDS BIOPROSTHESIS
FDA Adverse Event
Death
·EDWARDS LIFESCIENCES·Product code LWR·March 14, 2008
NC Traveler RX Coronary Dilatation Catheter, Part No. 1013152-12, 1013152-15, 1013152-20, 1013153-08, 1013153-12, 1013153-15, 1013153-20, 1013154-08, 1013154-12, 1013154-15, 1013154-20, 1013155-08, 1013155-12 1013155-15, 1013155-20, 1013156-12, 1013156-15, 1013157-08, 1013157-12, 1013157-15
FDA Recall
Terminated
·Abbott Vascular·Product code LOX·March 22, 2017