8 results
·
17ms
·
Sources: EU EUDAMED, US FDA
INSTRUMENT WARMER
FDA 510(k)
FDA Class 2
·General Hospital
MEGA PLUS MIS SPINE SYSTEM
FDA UDI
BK MEDITECH CO.,LTD.·08809665584304·MIS Fenestrated Screw, Ø5.5 x 30mm, Ø5.5mm Rod
PURITAN-BENNETT COMPANION 500 LIQUID OXYGEN SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
NOVA GAUZE(R) DISPOSABLE NONWOVEN SPONGES, STERILE
FDA 510(k)
FDA Class 2
·Neurology
STYLE 68 SALINE FILLED BREAST IMPLANT
FDA Adverse Event
Injury
·ALLERGAN (COSTA RICA)·Product code FWM·December 23, 2025
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·January 22, 2013
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 14, 2010
INTEGRITY AFX DR
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, CRMD·Product code DXY·January 15, 2014