7 results
·
34ms
·
Sources: EU EUDAMED, US FDA
MODEL 1100 COLD THERAPY DEVICE
FDA 510(k)
FDA Class 2
·Physical Medicine
LASER CRP KIT(C-REACTIVE PROTEIN REAGENTS)
FDA 510(k)
FDA Class 2
·Immunology
EZ-SCREEN:BARBITURATES
FDA 510(k)
FDA Class 2
·Clinical Toxicology
BD TRUCOUNT¿ ABSOLUTE COUNTING TUBES
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND COMPANY BD BIOSCIENCES·Product code GKZ·May 20, 2024
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·February 11, 2013
RIATA PASSIVE FIXATION
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·January 10, 2011
ACCU-CHEK ® MOBILE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·July 24, 2014