14 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Shockwave Medical Peripheral Intravascular Lithotripsy (IVL) System
FDA 510(k)
FDA Class 2
·Cardiovascular
BD Difco™ QC Antigen Shigella Group C1
FDA UDI
BECTON, DICKINSON AND COMPANY·00382902210412·Vial Qc Antigen Shigella Grp C1 1Ml
FareTec PST
FDA UDI
FARETEC, INC.·B54122210410·FareTec PST, Tactical, black with solid wheels ...
Integra® Miltex®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780424567·Integra® Miltex® Tydings Tonsil Snare, 9-3/4" S...
Atoll
FDA UDI
Seaspine Orthopedics Corporation·10889981033910·Head - Head Connector. The Atoll OCT Spinal Sys...
IQ FLEX M
FDA Adverse Event
Malfunction
·FIRST SOURCE INC.·Product code IZL·May 29, 2024
Wrist Blood Pressure Monitor, Model Name:W203, Wrist Blood Pressure Monitor, Model Name:W202, Wrist Blood Pressure Monitor, Model Name:W1681
FDA 510(k)
FDA Class 2
·Cardiovascular
WA RUBBERMATE LATEX POWDER-FREE EXAM GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 30, 2024
CONNECTOR HEAD TO HEAD - 48 MM
FDA Adverse Event
Other
·THEKEN SPINE·Product code KWP·June 8, 2010
COLLEAGUE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 23, 2011
VALIANT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·November 3, 2014
UNKNOWN
FDA Adverse Event
Injury
·ETHICON INC.·Product code FTL·July 11, 2013
X-Celerator Hydrophilic Exchange Guidewire Catalog No. 103-0601-300 103-0601-350V10 103-0602-350V06 103-0601-300V01 103-0602-300 103-0602-350V09 103-0601-300V02 103-0602-300V01 103-0602-350V10 103-0601-300V03 103-0602-300V02 103-0601-300V06 103-0602-300v06 103-0601-300V10 103-0602-300V09 103-0601-300V11 103-0602-300V10 103-0601-350 103-0602-350 103-0601-350V01 103-0602-350V01 103-0601-350V06 103-0602-350V02
FDA Enforcement
Class I
·Terminated·Micro Therapeutics Inc, Dba Ev3 Neurovascular·November 16, 2016