11 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
MoisturemeterD
FDA 510(k)
FDA Class 2
·Cardiovascular
VACCESS LT LONG-TERM HEMODIALYSIS CATHETER PLUS
FDA UDI
Bard Access Systems, Inc.·00801741010996·VACCESS PLUS, ST, 16 FR. 31cm
CRYONIZE TM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SYNTHES (USA) ELECTRIC PEN DRIVE SYSTEM
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
EPD 60000 RPM
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HWE·June 27, 2017
POWER LOAD
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FPO·June 3, 2013
MAESTRO SMALL FIXED DURAGUARD
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS-KALAMAZOO·Product code ERL·October 6, 2014
RADIAL JAW 4 BIOPSY FORCEPS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - COSTA RICA·Product code FCL·June 28, 2011
DRILL BIT Ø1.8 F/MATMAND L125 2FLUTE F/0
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code DZI·September 3, 2013
CABLE 3M TO CONSOLE
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HWE·October 16, 2014
INTIMA II¿ CLOSED IV CATHETER SYSTEM
FDA Adverse Event
Malfunction
·BD (SUZHOU)·Product code FOZ·October 31, 2018