8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
AMSINO SUTURE REMOVAL KIT
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
CT LUCIA
FDA UDI
CARL ZEISS MEDITEC PRODUCTION, LLC·00843045100775·3-piece, monofocal, hydrophobic, acrylic, intra...
ENVAN HEART RATE MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
EMBRYON GIFT TRANSFER CATHETERS/SETS
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
AV LOOP KIT
FDA Adverse Event
Malfunction
·TRANSONIC SYSTEMS, INC.·Product code DXG·March 14, 2013
INTRINSIC
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code LWS·April 12, 2011
RIATA ST ACTIVE FIXATION
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 27, 2008
Belmont Rapid Infuser, a Fluid Management System, Model FMS2000.
FDA Enforcement
Class II
·Terminated·Belmont Instrument Corporation·October 24, 2012