7 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
COREPASS Modular Microcatheter (FLEX); COREPASS Modular Microcatheter (CONTROL)
FDA 510(k)
FDA Class 2
·Cardiovascular
Nitrile Powder Free Examination Glove (Blue)
FDA 510(k)
FDA Class 1
·General Hospital
CONFLUENT SURGICAL DUAL LIQUID APPLICATOR, MODEL 70-2005093
FDA 510(k)
FDA Class 2
·General Hospital
PRECISION XTRA/OPTIUM
FDA Adverse Event
Injury
·ABBOTT DIABETES CARE INC, USA·Product code LFR·November 21, 2008
DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·September 10, 2011
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 23, 2013
ATLAS GOLD
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·December 18, 2023