7 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
CMDR-2ST & CMDR-2SLWT DIGITAL PORTABLE X-RAY
FDA 510(k)
FDA Class 2
·Radiology
INNOVATOR X
FDA Adverse Event
Injury
·OSSUR MEXICO·Product code IOY·December 21, 2020
BIOFLEX LD-175 AND LD-1200 TREATMENT HEADS
FDA 510(k)
FDA Class 2
·Physical Medicine
MEDTRONIC C315 DELIVERY CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013
RHEUMATOID FACTOR TEST SYSTEM
FDA Adverse Event
Injury
·BECKMAN COULTER INC.·Product code DHR·June 28, 2011
VERSACARE
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·September 3, 2008