16 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ACUFEX SCREW CANNULA
FDA 510(k)
FDA Class 2
·Orthopedic
TIPSEP-T4(RIA) T4 RADIOIMMUNOASSAY
FDA 510(k)
FDA Class 2
·Clinical Chemistry
PLAC TEST REAGENT KIT,CALIBRATOR KIT, LP-PLA2 CONTROL KIT, MODEL(S) 90107,90109,90109
FDA 510(k)
FDA Class 2
·Immunology
PIPELINE EMBOLIZATION DEVICE
FDA Adverse Event
Injury
·EV3 NEUROVASCULAR·Product code OUT·February 21, 2013
DISTAL END CUTTER
FDA Adverse Event
Malfunction
·DENTSPLY GAC·Product code EJB·January 18, 2011
ANCHOR L SCREWDRIVER MODULAR FLEXIBLE
FDA Adverse Event
Malfunction
·STRYKER SPINE-FRANCE·Product code LXH·August 1, 2014
NSK
FDA Adverse Event
Injury
·NAKANISHI INC.·Product code EGS·April 26, 2018
COD.712 TOP CIRC.RACC.CARDIO
FDA Adverse Event
Other
·SORIN GROUP ITALIA·Product code DTN·December 15, 2011
NSK
FDA Adverse Event
Injury
·NAKANISHI, INC.·Product code EGS·May 12, 2015
NSK
FDA Adverse Event
Malfunction
·NAKANISHI INC.·Product code EGS·October 9, 2025
NSK
FDA Adverse Event
Injury
·NAKANISHI INC.·Product code EGS·December 19, 2016
NSK
FDA Adverse Event
Injury
·NAKANISHI INC.·Product code EGS·March 1, 2018
NSK
FDA Adverse Event
Injury
·NAKANISHI INC.·Product code EGS·January 15, 2018
NSK
FDA Adverse Event
Injury
·NAKANISHI INC.·Product code EGS·June 6, 2018
DA-800C5L
FDA Adverse Event
Injury
·NAKANISHI INC.·Product code EGS·May 2, 2016
NSK
FDA Adverse Event
Injury
·NAKANISHI INC.·Product code EGS·April 26, 2018