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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