24 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EchoSolv AS
FDA 510(k)
FDA Class 2
·Radiology
J & J INSTRUMENTS
FDA UDI
J & J INSTRUMENTS INC·00817524026108·CRILE FCP 5.5"" CVD
ETEX MIXING AND DELIVERY SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
PTA Balloon Dilatation Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
BD INSYTE AUTOG BC WING
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·December 5, 2024
BD INSYTE AUTOG BC WING
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·December 5, 2024
BD INSYTE AUTOG BC WING
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·December 6, 2024
SPIDERFX EMBOLIC PROTECTION DEVICE
FDA Adverse Event
Injury
·EV3 INC.·Product code NTE·November 7, 2008
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 18, 2011
DIMENSION® CLINICAL CHEMISTRY SYSTEM
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code MLM·July 22, 2013
SPECTRA OPTIA
FDA Adverse Event
Injury
·TERUMO BCT·Product code GKT·June 2, 2017
SPECTRA OPTIA
FDA Adverse Event
Injury
·TERUMO BCT·Product code LKN·June 2, 2017
COBE SPECTRA BLOOD COLLECTION
FDA Adverse Event
Injury
·TERUMO BCT·Product code GKT·May 30, 2017
PIPELINE EMBOLIZATION DEVICE
FDA Adverse Event
Injury
·EV3 NEUROVASCULAR·Product code OUT·December 18, 2013
PINN MULTIHOLE W/GRIPTION 50MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code KWA·March 15, 2023
PLATE, FIXATION, BONE
FDA Adverse Event
Injury
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·March 1, 2018
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·March 1, 2018
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·May 22, 2015
BD INSYTE AUTOG BC WING
FDA Adverse Event
Malfunction
·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 12, 2024
PRODIGY AUTOCODE
FDA Adverse Event
Injury
·OK BIOTECH CO., LTD.·Product code NBW·June 1, 2017