194 results
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29ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MED-TEC BELLYBOARD, MODELS MT-BBA-01 & MT-BBA-02
FDA 510(k)
FDA Class 2
·Radiology
N.A.
FDA UDI
DENTAURUM GmbH & Co.KG·J011023293000·Hard metal tip for ligator (023-292-00)
EXCITE DSC
FDA 510(k)
FDA Class 2
·Dental
NIPRO HYPODERMIC NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
SPACEMAKER PREPERITONEAL DIST BALLOON
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY USSC PUERTO RICO·Product code GCJ·February 28, 2013
NEXGEN LPS-FLEX GSF FEMORAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·February 15, 2011
ENDO CLIP 5MM CLIP APPLIER
FDA Adverse Event
Injury
·NORTH HAVEN - USS·Product code GDO·April 1, 2008
PS FEMORAL COMPONENT CLOSED BOX LGE RIGHT 74 MM CEMENTED
FDA Adverse Event
Malfunction
·BIOMET SPAIN, S.L.·Product code JWH·June 3, 2020
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 12, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 2, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
VANGUARD DA 360 KNEE SYSTEM ARCOM TIBIAL BEARING 63/67 X 18MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·October 20, 2016
VG DA 360 O/S TIB TRAY COCR 63
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·June 2, 2016
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
ZYGOMATIC IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·September 23, 2024