15 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Polux , Minerva and Atropos PTA Balloon Dilatation Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613084875·K-Wire, Double Ended, Trocar Point, Diameter 0....
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613084837·K-Wire, Double Ended, Trocar Point, Diameter 0....
Monza Cervical Plate System
FDA UDI
Altus Spine, LLC·B41711602561·56mm Cervical Plate, 2 Level
3M™ Unitek™
FDA UDI
3M UNITEK CORPORATION·00652221044778·Unitek(TM) Molar Band General Purpose Narrow Re...
VIAL SUREPATH COLLECTION KIT 500
FDA Adverse Event
Malfunction
·TRIPATH IMAGING, INC·Product code MKQ·April 20, 2023
THE IC-PRO SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
UNICEL DXC 600I SYNCHRON ACCESS CLINICAL SYSTEM
FDA 510(k)
FDA Class 2
·Clinical Chemistry
GORE DRYSEAL FLEX INTRODUCER SHEATH
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code DYB·October 19, 2020
GORE® DRYSEAL FLEX INTRODUCER SHEATH
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code DYB·October 6, 2016
HOMECHOICE PRO
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·June 10, 2013
MARQUIS SERIES STOPCOCK
FDA Adverse Event
Malfunction
·MERIT MEDICAL SYSTEMS, INC.·Product code DTL·June 2, 2011
COLLEAGUE CX VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 16, 2008
SPECTRA WAVEWRITER?
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·April 4, 2025
GORE® DRYSEAL FLEX INTRODUCER SHEATH
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code DYB·May 30, 2023