12 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
MESH, SURGICAL, POLYMERIC
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
N/A
FDA UDI
Key Scientific Products Incorporated·00850041798028·PEP REAGENT
N/A
FDA UDI
Key Scientific Products Incorporated·00850041798042·Pep ReagentT
ACTIFUSE BONE GRAFT SUBSTITUTE AND ABX E-Z-FIL AND SHAPE BONE GRAFT SUBSTITUTES
FDA 510(k)
FDA Class 2
·Orthopedic
Jaysun Powder Free Vinyl Patient Examination Gloves, Clear (non-colored)
FDA 510(k)
FDA Class 1
·General Hospital
IMP CBL DIA2 SS CABLE SLEEVE
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code JDQ·November 18, 2016
IMP CBL DIA2 SS CABLE SLEEVE
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code JDQ·November 18, 2016
IMP CBL DIA2 SS &CABLE SLEEV
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code JDQ·November 30, 2016
IMP CBL DIA2 SS & CABLE SLEEVE
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code JDQ·July 20, 2016
MUSTANG¿
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code LIT·February 28, 2013
ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORP.·Product code LZG·January 12, 2011
TAIGA 6F GUIDE CATHETER
FDA Adverse Event
Malfunction
·MEDTRONIC, INC·Product code DQY·August 6, 2014