16 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
JAW INS.BIP.MARYLAND DISS.FEN.5/310MM
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code GEI·July 21, 2016
JAW INS.BIP.MACRO FORCEPS D: 5/310MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO KG TUTTLINGEN 78532·Product code GEI·December 12, 2014
BIPOLAR MACRO FORCEPS D:5/ 310MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO KG·Product code GEI·April 6, 2015
JAW INS. BIP. MARYLAND DISS. FCPS 5/310MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code GEI·January 14, 2015
BIPOLAR MARYLAND DISS.FCPS 5MM 310MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO KG·Product code GEI·March 9, 2015
JAW INS.BIP.MARYLAND DISS.FEN.5/310MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code GEI·August 29, 2014
JAW INS. BIP.MARYLAND DISS.FEN.5/310MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG.·Product code GEI·January 13, 2015
MARYLAND GSP.FORCEPS FEN.5/310MM HF CON.
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code GEI·February 19, 2014
JAW INS.BIP.MARYLAND DISS.FEN.5/310MM
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code GEI·October 25, 2016
JAW INS.BIP.MARYLAND DISS.FEN.5/310MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code GEI·August 13, 2015
JAW INS.BIP.MARYLAND DISS.FEN.5/310MM
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code GEI·May 10, 2016
2520274-2013-10151
FDA Adverse Event
Malfunction
·Product code KTT·February 28, 2013
CONTOUR CURVED CUTTER STAPLER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.·Product code GDW·February 14, 2008
JAW INS.BIP.MARYLAND DISS.FEN.5/310MM
FDA Adverse Event
Malfunction
·AESCULAP AG·Product code GEI·October 27, 2016
JAW INS. BIP. MARYLAND DISS.FCPS 5/310MM
FDA Adverse Event
Malfunction
·AESCULAP, INC.·Product code GEI·July 30, 2015
MARYLAND GSP.FORCEPS FEN.5/310MM HF.CON.
FDA Adverse Event
Malfunction
·AESCULAP, INC.·Product code GEI·August 21, 2015