8 results
·
20ms
·
Sources: EU EUDAMED, US FDA
GenaCheck COVID-19 Rapid Self-Test
FDA 510(k)
FDA Class 2
·Microbiology
Philips
FDA UDI
Sbo Hearing A/S·05714464089086·HEARLINK 1500 CIC
16 ch Tx/Rx Knee SPEEDER
FDA 510(k)
FDA Class 2
·Radiology
ACCU-SOURCE
FDA 510(k)
FDA Class 2
·Radiology
NXSTAGE SYSTEM ONE
FDA Adverse Event
Injury
·NXSTAGE MEDICAL, INC.·Product code KDI·December 3, 2008
MINICAP TRANSFSET
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·September 16, 2011
OBTRYX SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·July 29, 2013
COBAS® DPX - 192T
FDA Adverse Event
Malfunction
·ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG·Product code QHO·September 17, 2025