213 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
VORTRAN GO2VENT with PEEP Valve
FDA 510(k)
FDA Class 2
·Anesthesiology
Nucleus
FDA UDI
COCHLEAR LIMITED·09321502017756·Cochlear Nucleus CP800 Series Compact Rechargea...
IDB 3
FDA UDI
Sprintray, Inc.·00850070544832·SprintRay IDB 3 is a light-curable polymerizabl...
VEO® Lateral Interbody Fusion System
FDA UDI
Choice Spine, LP·00840996132749·LATERAL,NERVE RETRACTOR
WANDY SELF-ADHESIVE NEUROSTIMULATION ELECTRODE
FDA 510(k)
FDA Class 2
·Neurology
EXOMIO, MODEL 1.1
FDA 510(k)
FDA Class 2
·Radiology
670G INSULIN PUMP MMT-1780KL
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·December 5, 2022
MINIMED 780G OUS SYSTEM BLE CONNECT 3.0 MMOL/L
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·June 22, 2023
AUTOMATED IMPELLA CONTROLLER
FDA Adverse Event
Malfunction
·ABIOMED, INC.·Product code OZD·November 3, 2024
630G INSULIN PUMP MMT-1715K 630G BLACK MG
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·January 25, 2022
PUMP MMT-1712KL 640G V4.10 BK SF MG
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 14, 2022
670G INSULIN PUMP MMT-1780KL
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·April 14, 2022
PUMP MMT-1782K 670G V4.11 MM
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·March 3, 2022
PUMP MMT-1711KL 640G V4.10 BK SF MM
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·February 24, 2022
630G INSULIN PUMP MMT-1715K 630G BLACK MG
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·February 1, 2022
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·September 1, 2021
MINIMED 770G US SYSTEM BLE CONNECT 3.0 MG/DL
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·January 12, 2023
PROLIEVE THERMODILITATION KIT
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code MEQ·October 16, 2008
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR·Product code CBK·June 28, 2013
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 5, 2011