8 results
·
25ms
·
Sources: EU EUDAMED, US FDA
CEDIA FERRITIN ASSAY
FDA 510(k)
FDA Class 2
·Immunology
APEX PS Knee
FDA UDI
Omni Life Science, Inc.·00841690113195·PS Insert, Size 3 x 18mm
Instrument Case
FDA UDI
KATENA PRODUCTS, INC.·00841668110935·STERILIZING CASE NARROW
VIVI ERGON-X HF
FDA 510(k)
FDA Class 2
·Dental
SCIVOLUTIONS VARIOUS ANTIBACTERIAL BANDAGES
FDA 510(k)
FDA Unclassified
·Unknown
DEXCOM G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM, DEXCOM SHARE SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·July 16, 2015
KYPHX® HV-R¿ BONE CEMENT
FDA Adverse Event
Injury
·MEDTRONIC SPINE LLC·Product code NDN·December 10, 2010
HEARTSTART MRX
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·December 17, 2012