29 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
APEX PS Knee
FDA UDI
Omni Life Science, Inc.·00841690113225·PS Insert, Size 4 x 11mm
RR - UP - Commuter Passenger - zlb
FDA UDI
Certified Safety Manufacturing, Inc.·00766588024110·RR - UP - Commuter Passenger - zlb
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B1676220411070·
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B1676220411150·
X SERIES
FDA UDI
Zoll Medical Corporation·00847946018672·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...
X SERIES
FDA UDI
Zoll Medical Corporation·00847946005948·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...
X SERIES
FDA UDI
Zoll Medical Corporation·00847946014896·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B1676220411000·
X SERIES
FDA UDI
Zoll Medical Corporation·00847946019105·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...
X SERIES
FDA UDI
Zoll Medical Corporation·00847946012601·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...
X SERIES
FDA UDI
Zoll Medical Corporation·00847946061333·X SERIES, MONITOR/DEFIBRILLATOR, 12 LD W/ INTER...
NUVASIVE TRIAD FACET SCREW SYSTEM
FDA 510(k)
FDA Unclassified
·Unknown
Z6/Z60/Z60T/Z60S/Z60 Pro/DP-60 Diagnostic Ultrasound System
FDA 510(k)
FDA Class 2
·Radiology
VERSACROSS CONNECT LAAC ACCESS SOLUTION
FDA Adverse Event
Injury
·BAYLIS MEDICAL COMPANY INC.·Product code DRE·April 6, 2023
SPECTRUM IQ INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·March 23, 2022
SPECTRUM IQ INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·June 13, 2022
SPECTRUM IQ INFUSION PUMP
FDA Adverse Event
Injury
·BAXTER HEALTHCARE CORPORATION·Product code FRN·May 25, 2022
K 520411-2, Hercep Test, 35Test, HER2, Protein
FDA Recall
Terminated
·Dakocytomation California Inc·Product code MVC·September 29, 2005
STARCLOSE VASCULAR CLOSURE SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR REDWOOD CITY·Product code MGB·November 4, 2008