13 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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KD-525E FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
Mizzy Fleck's
FDA UDI
Keystone Industries·H66860703951·Bulk PCA Cement Powder
CM-hex screw system
FDA UDI
Cendres+Métaux SA·07640173093602·CM-hex screw system
Pin screw
Spiral drill Ø 1....
LINEAR 3-6
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·November 19, 2020
INFINION CX
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·January 29, 2024
E-POWER
FDA 510(k)
FDA Class 2
·Physical Medicine
EINSTEIN PROCESSING AND REVIEW WORKSTATION
FDA 510(k)
FDA Class 2
·Radiology
ASR TAP SLV ADAP 12/14 -1
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD.·Product code KWA·March 17, 2016
LEAD MODEL 302
FDA Adverse Event
Malfunction
·CYBERONICS INC·Product code LYJ·April 22, 2013
ACCU-CHEK FLEXLINK PLUS INFUSION SET
FDA Adverse Event
Malfunction
·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code FRN·April 18, 2011
GE OEC 7600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·July 9, 2008
COCR FEMORAL HEAD 32 SIZE M
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL, SA·Product code LZO·July 3, 2013
Belmont Rapid Infuser, a Fluid Management System, Model FMS2000.
FDA Enforcement
Class II
·Terminated·Belmont Instrument Corporation·October 24, 2012