13 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SPECTRUM SPINE FENESTRATED FACET SCREW SYSTEM
FDA 510(k)
FDA Unclassified
·Unknown
NexxZr™ T / D-100-18-NT-C300-SD
FDA UDI
SAGEMAX BIOCERAMICS, INC·00842271113368·
GENUINE FIRST AID CPR MASK
FDA 510(k)
FDA Class 2
·Anesthesiology
PROMOS SHOULDER
FDA 510(k)
FDA Class 2
·Orthopedic
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·May 29, 2025
COBAS 6000 C501 MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code CEM·May 19, 2008
MPACT FLAT PE HC LINER Ø 32 / D
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LPH·December 2, 2016
COBAS INTEGRA 800
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·February 26, 2010
ORTHO SUMMIT SAMPLE HANDLING SYSTEM
FDA Adverse Event
Malfunction
·HAMILTON BONADUZ AG·Product code MMH·May 29, 2013
ACCESS 2 IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·June 17, 2011
GORE PROPATEN VASCULAR GRAFT (STRETCH SMALL DIAMETER)
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code DSY·August 21, 2008
TRUEMETRIX
FDA Adverse Event
Malfunction
·TRIVIDIA HEALTH, INC.·Product code NBW·June 13, 2019
TRUE METRIX
FDA Adverse Event
Injury
·TRIVIDIA HEALTH INC·Product code NBW·December 28, 2020