15 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ECHELON Oval V6.2 MRI System
FDA 510(k)
FDA Class 2
·Radiology
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B1676221619150·
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B1676221619000·
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B1676221619070·
BD BACTEC¿ MGIT¿ 960 SUPPLEMENT KIT
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·May 7, 2025
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·May 19, 2015
NUVASIVE POLYAXIAL SPINAL SCREWS
FDA 510(k)
FDA Class 2
·Orthopedic
EndoTool IV System
FDA 510(k)
FDA Class 2
·Anesthesiology
UNKNOWN IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code MHY·May 19, 2015
GALILEO ECHO
FDA Adverse Event
Malfunction
·IMMUCOR, INC.·Product code KSZ·May 31, 2016
GALILEO ECHO
FDA Adverse Event
Malfunction
·IMMUCOR, INC.·Product code KSZ·June 2, 2016
OPTICROSS?
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - FREMONT (SUD)·Product code OBJ·November 3, 2014
OMNIPOD INSULIN PUMP
FDA Adverse Event
Injury
·INSULET CORPORATION·Product code LZG·August 19, 2011
OCTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 9, 2013
BD BACTEC¿ MGIT¿ 960 SUPPLEMENT KIT
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·March 19, 2025