10 results
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19ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Vanguard Dental Unit
FDA 510(k)
FDA Class 1
·Dental
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523138203·Trial, 34 X 28, 17mm Height 28° Hyperlordotic
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523138227·Trial, 34 X 28, 21mm Height 28° Hyperlordotic
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523138210·Trial, 34 X 28, 19mm Height 28° Hyperlordotic
MYSAFETY SYRINGE
FDA 510(k)
FDA Class 2
·General Hospital
VISIONSCOPE HIGH DEFINITION ENDOSCOPY CAMERA SYSTEM WITH; CAMERA CONTROL UNIT; CAMERA HANDPIECE; VISIONSCOPE ENDOSCOPES
FDA 510(k)
FDA Class 2
·Orthopedic
STENT - VASCULAR RECONSTRUCTION
FDA Adverse Event
Injury
·CODMAN AND SHURTLEFF, INC·Product code NJE·April 30, 2018
STENOSCOP
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 3, 2013
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code MDS·July 8, 2011
PROTECTA XT CRT-D
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·October 10, 2014