10 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·July 11, 2024
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·September 25, 2024
JAW INS. BULLET NOSE GRASPER 5MM 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
DISSECTOR CEV531-3 DIA 5MM LRG CVD
FDA Adverse Event
Injury
·INTEGRA MICROFRANCE S.A.S.·Product code GEI·June 7, 2019
SELOX JT 45
FDA Adverse Event
Injury
·BIOTRONIK SE & CO. KG·Product code NVN·March 12, 2013
EON MINI IPG, 16-CHANNEL RECHARGEABLE
FDA Adverse Event
Injury
·ST JUDE MEDICAL - NEUROMODULATION PULSE GENERATOR·Product code LGW·February 17, 2011
KINSA SUTURE ANCHOR SYSTEM, MACHINED PEEK
FDA Adverse Event
Malfunction
·SMITH & NEPHEW INC., ENDOSCOPY DIV.·Product code MBI·February 19, 2008
IMP,TSV,4.7,8,MTX,MG
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·January 14, 2022
BIFURCATED EXT SET
FDA Adverse Event
Malfunction
·VYGON USA·Product code FPA·August 19, 2020