25 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SONATHERM 600I ULTRASONIC LESION GENERATING SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
APEXPRO TELEMETRY SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
MODIFICATION TO:LAPAROSCOPIC/ENDOSCOPIC INSTRUMENT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PROXIMATE RELOADABLE LINEAR CUTTER WITH SAFETY LOCK-OUT
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, INC.·Product code GAG·March 22, 2006
ENDOPATH ETS45 ENDOSCOPIC LINEAR CUTTER - 3.5MM
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.·Product code KOG·June 16, 2006
ENDOPATH ETS FLEX45 ENDOSCOPIC ARTICULATING LINEAR
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code GDW·June 13, 2006
ENDOPATH ETS FLEX45 ENDOSCOPIC ARTICULATING LINEAR
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code GCJ·June 8, 2006
ENDOPATH ETS FLEX45 ENDOSCOPIC ARTICULATING LINEAR
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code GCJ·June 19, 2006
ENDOPATH ETS FLEX45 ENDOSCOPIC ARTICULATING LINEAR CUTTER
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GCJ·June 8, 2006
45MM ARTICING LNR CUTR/BLUE RLD
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, INC.·Product code GCJ·December 21, 2005
ENDO LINEAR CUTTERS-ETS45MM
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code KOG·June 8, 2006
ENDOPATH ETS-FLEX45 ARTICULATING ENDOSCOPIC LINEAR
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GDW·June 15, 2006
ENDOPATH ETS45 ENDOSCOPIC LINEAR CUTTER - 2.5 MM -
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code KOG·October 21, 2005
ETS 45 ENDO LINEAR CUTTER BL
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code KOG·December 19, 2005
NV GXL LINR, NTRL, 32MM ID, GROUP 2 CUPS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code MEH·July 20, 2022
V40 FEM HEAD ORTHINOX 28+4
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·April 22, 2013
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·April 14, 2011
2600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·July 9, 2008
NV GXL LNR, LIPPED, 36MM ID, GROUP 3 CUPS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JDI·July 9, 2024
ENDOPATH ETS FLEX45 ENDOSCOPIC ARTICULATING LINEAR CUTTER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code GDW·June 8, 2006