10,000 results
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32ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MPV
FDA UDI
Movair, Inc.·00860013561406·
MPV
FDA UDI
Movair, Inc.·00860013561413·
HOVEROUND MPV
FDA 510(k)
FDA Class 2
·Physical Medicine
HOVEROUND MPV-5 POWERCHAIR
FDA 510(k)
FDA Class 2
·Physical Medicine
D3 Fastpoint
FDA UDI
DIAGNOSTIC HYBRIDS, INC.·30014613330813·D3 FASTPOINT RSV/MPV KIT
RDW AND MPV INDICES ON HEMAT 12
FDA 510(k)
FDA Class 2
·Hematology
MPV-7201 NON-INVASIVE BLOOD PRESSURE MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
EXTRUDE MPV
FDA Adverse Event
Injury
·KERR CORP.·Product code ELW·August 28, 2003
CELL-DYN RUBY ANALYZER
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·March 6, 2012
CELL-DYN SAPPHIRE ANALYZER
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·August 24, 2009
HOVEROUND MPV-4
FDA Adverse Event
Death
·HOVEROUND CORP.·Product code ITI·October 15, 2004
CELL-DYN RUBY ANALYZER
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·April 7, 2009
UNICEL DXH 800 COULTER CELLULAR ANALYSIS SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code GKZ·January 6, 2026
MPV, 7200SPE, W/PSV
FDA Adverse Event
Injury
·CARLSBAD-RX·Product code CBK·August 15, 2008
COULTER LH 500 HEMATOLOGY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GKZ·September 26, 2014
CDS/R/4K DILUENT/SHEATH, 20L
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIVISION / CELLDYN·Product code GKL·January 4, 2007
CDS/R/4K DILUENT/SHEATH, 20L
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIV/CELLDYN·Product code GKL·January 8, 2007
CDS/R/4K DILUENT/SHEATH, 20L
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS·Product code GKL·January 4, 2007
CELL-DYN DILUENT/SHEATH
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKL·January 5, 2007
CDS/R/4K DILUENT/SHEATH, 20L
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIV/CELLDYN·Product code GKL·January 4, 2007