27 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SELLAS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MEDISLIM
FDA Adverse Event
Injury
·MEDICREATIONS, LLC·Product code GEX·April 27, 2020
BD INSYTE AUTOGUARD SHIELDED IV CATHETER
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·August 27, 2020
100 SERIES OXYGEN ANALYZER, MODELS 1000-E AND 1000-I
FDA 510(k)
FDA Class 2
·Anesthesiology
BLUE SENSOR, DISPOSABLE ECG ELECTRODES FOR ANAESTHESIA
FDA 510(k)
FDA Class 2
·Cardiovascular
INSYTE CATHETER
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·March 31, 2021
INSYTE AUTOGUARD YEL 24GA X .75IN
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·December 9, 2020
BD INSYTE AUTOGUARD SHIELDED IV CATHETER
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·October 6, 2020
BD INSYTE AUTOGUARD SHIELDED IV CATHETER
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·August 26, 2020
BD INSYTE AUTOGUARD SHIELDED IV CATHETER
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·August 26, 2020
BD INSYTE AUTOGUARD SHIELDED IV CATHETER 24GA 0.75IN (0.7 X 19 MM)
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·September 23, 2020
VERCISE CARTESIA
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code NHL·May 13, 2021
INSYTE AUTOGUARD YEL 24GA X .75IN
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·December 10, 2020
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·April 26, 2013
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·May 6, 2011
MST8 FINAL ASSY JRZ
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code KNW·July 24, 2008
ONYX
FDA Adverse Event
Injury
·COVIDIEN (IRVINE)·Product code MFE·April 21, 2015
GUIDEWIRE MODEL UNKNOWN
FDA Adverse Event
Injury
·COVIDIEN (IRVINE)·Product code DQX·April 21, 2015
ONYX
FDA Adverse Event
Death
·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·October 1, 2024
BD INSYTE AUTOGUARD SHIELDED IV CATHETER 24GA 0.75IN (0.7 X 19 MM)
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·August 13, 2020