8 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BreathID Hp Lab System, BreathID Smart System
FDA 510(k)
FDA Class 1
·Microbiology
MODIFICATION TO M2376A DEVICELINK SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
DISPOSABLE ADHESIVE SURFACE ELECTRODE
FDA 510(k)
FDA Class 2
·Neurology
VERSACROSS CONNECT LAAC ACCESS SOLUTION
FDA Adverse Event
Injury
·BAYLIS MEDICAL COMPANY INC.·Product code DRE·April 6, 2023
4 FR SINGLE LUMEN GROSHONG NXT CLEARVUE BASIC KIT
FDA Adverse Event
Injury
·C. R. BARD INC. (BASD)·Product code LJS·November 4, 2008
TI STANDARD PEDICLE BOLT
FDA Adverse Event
Malfunction
·ALPHATEC SPINE INC·Product code MNH·August 23, 2011
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 11, 2013
VERSACROSS CONNECT LAAC ACCESS SOLUTION
FDA Adverse Event
Injury
·BAYLIS MEDICAL COMPANY INC.·Product code DXF·April 25, 2023