4,006 results
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48ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LF900
FDA UDI
DAESUNG MAREF CO.,LTD.·08809315677455·Main device 1ea, OVERLAPPING LEG SLEEVE Small X...
LF400
FDA UDI
DAESUNG MAREF CO.,LTD.·08809802640252·Main device 1ea, OVERLAPPING LEG SLEEVE Small X...
LF900
FDA UDI
DAESUNG MAREF CO.,LTD.·08809802644540·Main device 1ea, OVERLAPPING LEG SLEEVE Small X...
LF900
FDA UDI
DAESUNG MAREF CO.,LTD.·08809802643406·Device 1ea , SXW401 2ea , Double Hose 1ea, Sing...
OMRON BLOOD PRESSURE MONITOR
FDA Adverse Event
Injury
·OMRON HEALTHCARE·Product code DXN·August 19, 2010
PARIETEX OPTIMIZED COMPOSITE MESH (PCO-OSX REFERENCES)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PROGRAMMING SOFTWARE
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·September 3, 2015
1-DAY ACUVUE TRUEYE (NARA A)
FDA Adverse Event
Injury
·JOHNSON & JOHNSON VISION CARE, INC. ¿ US·Product code LPL·August 5, 2016
PROGRAMMING SOFTWARE
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·March 15, 2016
PROGRAMMING SOFTWARE
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·July 1, 2014
PROGRAMMING SOFTWARE
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·June 25, 2015
PROGRAMMING SOFTWARE
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·July 3, 2013
SILICONE GEL BREAST IMPLANTS
FDA Adverse Event
Injury
·SQ·Product code FTR·July 26, 2000
TRIAGE CARDIAC HS TNI PANEL
FDA Adverse Event
Malfunction
·QUIDEL CARDIOVASCULAR INC.·Product code MMI·April 10, 2026
TRIAGE CARDIAC HS TNI PANEL
FDA Adverse Event
Malfunction
·QUIDEL CARDIOVASCULAR INC.·Product code MMI·April 10, 2026
TRIAGE CARDIAC HS TNI PANEL
FDA Adverse Event
Malfunction
·QUIDEL CARDIOVASCULAR INC.·Product code MMI·April 10, 2026
RENU (UNK TYPE)
FDA Adverse Event
Injury
·BAUSCH & LOMB INC.·Product code LPN·January 2, 2007
BD Biosciences MultiSET Flow Cytometry Software Versions 2.1, 2.1.1, and 2.2 with OS X operating systems, BD Biosciences, San Jose, CA 95131.
FDA Recall
Terminated
·BD Biosciences·Product code GKZ·September 6, 2007
CELLQUEST PRO SW
FDA Adverse Event
Malfunction
·BD BIOSCIENCES·Product code GKZ·August 31, 2007
ACUVUE OASYS BRAND CONTACT LENSES
FDA Adverse Event
Injury
·Product code LPL·September 17, 2014