21 results
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33ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EchoGo
FDA UDI
ULTROMICS LIMITED·05060634690041·
EchoGo
FDA UDI
ULTROMICS LIMITED·05060634690065·
EchoGo
FDA UDI
ULTROMICS LIMITED·05060634690058·
EchoGo
FDA UDI
ULTROMICS LIMITED·05060634690010·
EchoGo
FDA UDI
ULTROMICS LIMITED·05060634690072·
EchoGo
FDA UDI
ULTROMICS LIMITED·05060634690003·
EchoGo
FDA UDI
ULTROMICS LIMITED·05060634690027·
SYNCHROMED II
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·April 5, 2013
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·April 27, 2021
GORE® EXCLUDER® AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·April 28, 2022
GORE® EXCLUDER® AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·April 18, 2024
SUPER POLIGRIP ORIGINAL DENTURE ADHESIVE CREAM
FDA Adverse Event
Other
·GLAXOSMITHKLINE·Product code KOL·June 27, 2012
GORE® EXCLUDER® AAA ENDOPROSTHESIS
FDA Adverse Event
Death
·W.L. GORE & ASSOCIATES·Product code MIH·January 4, 2018
GORE® DRYSEAL FLEX INTRODUCER SHEATH
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code DYB·May 19, 2017
GORE® EXCLUDER® AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code MIH·October 20, 2015
SYNCHROMED II
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·March 16, 2022
HEARTMATE 3 LVAS IMPLANT KIT
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·April 30, 2021
GORE® TRI-LOBE BALLOON CATHETER
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code DQY·April 26, 2023
5 FR DL POWERPICC UPFT WITH MI AND TLS
FDA Adverse Event
Malfunction
·C. R. BARD INC. (BASD)·Product code LJS·May 10, 2011
CELL-DYN RUBY ANALYZER
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·August 13, 2018