14 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ViaValve Safety I.V. Catheter
FDA 510(k)
FDA Class 2
·General Hospital
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613017811·K-Wire, Double Ended, Trocar Point, Diameter Si...
Monza Cervical Plate System
FDA UDI
Altus Spine, LLC·B41711602351·35mm Cervical Plate, 2 Level
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613084837·K-Wire, Double Ended, Trocar Point, Diameter 0....
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613017828·K-Wire, Double Ended, Trocar Point, Diameter 0....
FILTEK SUPREME ULTRA FLOWABLE RESTORATIVE
FDA 510(k)
FDA Class 2
·Dental
ENDO-EASE ENDOSCOPIC OVERTUBE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
BD NEEDLE PRECISIONGLIDE 21X1IN
FDA Adverse Event
Malfunction
·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FMI·January 16, 2026
BD NEEDLE PRECISIONGLIDE 21X1IN
FDA Adverse Event
Malfunction
·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FMI·January 16, 2026
SYNCHROMED II
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·June 10, 2013
PARADIGM INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code LZG·September 19, 2014
SYNCHRON LX20 PRO SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·June 2, 2011
BD NEEDLE PRECISIONGLIDE 21X1IN
FDA Adverse Event
Malfunction
·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FMI·February 13, 2026
BD NEEDLE PRECISIONGLIDE 21X1IN
FDA Adverse Event
Malfunction
·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FMI·January 16, 2026