8 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MALLINCKRODT
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY TYCO HEALTHCARE·Product code BTR·August 16, 2012
LASER-FLEX(TM) TRACHEAL TUBE (CUFFED)
FDA 510(k)
FDA Class 2
·Anesthesiology
MALLINKRODT
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY TYCOHEALTHCARE·Product code JOH·August 17, 2010
ECG recorder and Arrhythmia Detector
FDA 510(k)
FDA Class 2
·Cardiovascular
ORTHO ANCHOR SCREWS
FDA 510(k)
FDA Class 2
·Dental
OT PING ENHANCED METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 14, 2014
GORE EXCLUDER AAA ENDOPROSTHESIS
FDA Adverse Event
Malfunction
·W. L. GORE & ASSOCIATES·Product code MIH·October 14, 2010
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP·Product code FRN·November 15, 2012