29 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SPIRA-C Open Matrix Cervical Interbody
FDA 510(k)
FDA Class 2
·Orthopedic
OsteoMed
FDA UDI
OSTEOMED LLC·00845694027335·2.4mm X 46mm Cannulated Headless Screw
OsteoMed
FDA UDI
OSTEOMED LLC·00845694069144·Cannulated 2.4 x 46mm Headless Screw Sterile Qty 2
TOMOTHERAPY TREATMENT SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
MOBIL-O-GRAPH NG 24 H ABP-CONTROL
FDA 510(k)
FDA Class 2
·Cardiovascular
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·August 6, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·August 6, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·August 6, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·October 17, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·November 9, 2018
ROSA ONE
FDA Adverse Event
Injury
·MEDTECH SA·Product code HAW·January 11, 2019
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·July 3, 2025
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code NAY·January 21, 2019
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·December 21, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code OLO·November 15, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code OLO·November 15, 2018
ARCOM 28MM RNGLOC LNR 10DEG24
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LPH·June 17, 2013
TOTALCARE BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·June 17, 2011
ROTABLATOR GUIDE WIRE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code MCX·September 19, 2008
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code OLO·November 15, 2018