8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
OROSPHERE HCDP
FDA 510(k)
FDA Class 2
·Dental
SIEMENS-ELEMA A.B. SERVO HUMIDIFIER 150
FDA 510(k)
FDA Class 1
·Anesthesiology
TANSCU O2
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PYRAMESH® IMPLANT SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code EZX·July 17, 2014
LAMITRODE 4
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·June 3, 2014
HYDRO THERMABLATOR (HTA) ENDOMETRIAL ABLATION SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code MNB·December 31, 2012
MYO CARDIOPLEGIA DELIVERY TUBE SETS
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code DTR·November 1, 2010
PYRAMESH IMPLANT SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code EZX·December 9, 2016