12 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SMV Scientific K-Wire and Pins
FDA 510(k)
FDA Class 2
·Orthopedic
DISCARDIT II 5ML WITH 24*1
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMF·November 7, 2019
POWDER FREE VINYL PATIENT EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
GRADIA CORE
FDA 510(k)
FDA Class 2
·Dental
ONE TOUCH ULTRA
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·October 10, 2003
QD11
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HBC·October 17, 2014
LAMITRODE TRIPOLE 16
FDA Adverse Event
Injury
·ST. JUDE MEDICAL -NEUROMODULATION·Product code LGW·June 14, 2013
BLADELESS VP 11MM ST W/ FIXATION
FDA Adverse Event
Malfunction
·UNITED STATES SURGICAL·Product code GCJ·July 28, 2011
MULTI-SIDEPORT DUAL CHECK VALVE CATHETER INFUSION SET
FDA Adverse Event
Injury
·COOK INC·Product code KRA·April 27, 2022
MULTI-SIDEPORT DUAL CHECK VALVE CATHETER INFUSION SET
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·April 11, 2022
MULTI-SIDEPORT DUAL CHECK VALVE CATHETER INFUSION SET
FDA Adverse Event
Malfunction
·COOK INC·Product code KRA·August 19, 2022
ALINITY I B12 REAGENT KIT
FDA Adverse Event
Malfunction
·A.I.D.D LONGFORD·Product code CDD·May 14, 2021