7 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
CORTICAL BONE SCREW
FDA 510(k)
FDA Class 2
·Orthopedic
Instrument Case
FDA UDI
KATENA PRODUCTS, INC.·00841668111086·INSTRUMENT CASE LARGE ALUMINUM
KASIOS TCP
FDA 510(k)
FDA Class 2
·Orthopedic
Infrared Therapy System
FDA 510(k)
FDA Class 2
·Physical Medicine
TOTALCARE BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·January 8, 2013
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORP·Product code LZG·December 23, 2010
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 17, 2014