8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
EMIT-AND METHOTREXATE CONTROL
FDA 510(k)
FDA Class 1
·Clinical Toxicology
MSI
FDA UDI
Modern Surgical Instruments LLC·00810130202881·Micro Discectomy Cervical Curette 8 1/2", fwd s...
GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 5/10 MM L
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·October 18, 2019
ACCESS CARDIOSYSTEMS MANUAL DEFIBRILLATOR
FDA 510(k)
FDA Class 2
·Cardiovascular
Rapid-i Kit
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
ASSURANT COBALT
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code NIO·May 15, 2014
CARELINK
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code DXY·October 31, 2012
HEARTSTART MRX-EMS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE·Product code MKJ·August 17, 2010