9 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
SURGAIRTOME TWO
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
ACTIFUSE BONE GRAFT SUBSTITUTE AND E-Z-FIL AND SHAPE BONE GRAFT SUBSTITUTE
FDA 510(k)
FDA Class 2
·Orthopedic
Rusch FloCath Quick 18 Fr. Coudé Hydrophilic Intermittent Catheter
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ESPRIT VENTILATOR
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, INC.·Product code CBK·April 30, 2014
2800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 5, 2012
SURESCAN
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·May 19, 2015
INDUCTIGRAFT
FDA Adverse Event
Injury
·BAXTER APATECH LTD·Product code MQV·January 16, 2014
INDUCTIGRAFT
FDA Adverse Event
Injury
·BAXTER APATECH LTD·Product code MQV·June 10, 2013
INDUCTIGRAFT
FDA Adverse Event
Injury
·BAXTER APATECH LTD·Product code MQV·February 16, 2012