33 results
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28ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CARDIO MED
FDA 510(k)
FDA Class 2
·Cardiovascular
Punch
FDA UDI
ADLER ORTHO SPA·08053617185228·PUNCH FOR TIBIA MB GENUS PANTHEON SZ. 3-4
ENDOFLIP
FDA 510(k)
FDA Class 2
·Orthopedic
STICK NET
FDA 510(k)
FDA Class 2
·Dental
PRIM SYM SET 2 CL W/FILTERTEK VALVE
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·March 21, 2012
PRIM SYM SET 2 CL W/FILTERTEK VALUE
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·February 21, 2012
PRIM SYM SET 2 CL W/FILTERTEK VALVE
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·July 9, 2012
PINNACLE MTL INS NEUT40IDX56OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·May 9, 2013
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·September 19, 2014
ADVIA CENTAUR XP HBC TOTAL (HBCT)
FDA Adverse Event
SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code LOM·May 26, 2011
PRIM SYM SET 2 CL W/FILTERTEK VALVE
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·February 14, 2012
PRIM SYM SET 2 CL W/FILTERTEK VALVE
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·July 5, 2012
PRIM SYM SET 2 CL W/FILTERTEK VALVE
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·July 5, 2012
PRIM SYM SET 2 CL W/FILTERTEK VALVE
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·July 5, 2012
PRIM SYM SET2 CL W/FILTERTEK VALVE
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·July 5, 2012
PRIM SYM SET 2 CL W/ FILTERTEK VALVE
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·July 5, 2012
PRIM SYM SET 2 CL W/FILTERTEK VALVE
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD·Product code FPA·January 16, 2012
PRIM SYM 2 CL W/FILTERTEK VALVE
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FPA·February 21, 2012
PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAW·February 27, 2024
VERTEBRAL DISTRACTOR
FDA Adverse Event
Malfunction
·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code LXH·December 10, 2018