6 results
·
25ms
·
Sources: EU EUDAMED, US FDA
JAIN BLOOD SHIELD
FDA 510(k)
FDA Class 2
·General Hospital
SENTRY SEMIAUTOMATIC EXTERNAL DEFIBRILLATOR; EXTERNAL DEFIBRILLATION PADS (ELECTRODES) DDP-100; BATTERY PACK 1200MAH; BA
FDA 510(k)
FDA Class 3
·Cardiovascular
BD Trek Powered Bone Biopsy System
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK INC·Product code NEK·December 3, 2010
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·July 3, 2014
HEARTSTART MRX - EMS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·December 6, 2012