33 results
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23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DISPOSABLE BLLOD COLLECTION NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
BABIES BEST WATER TEETHER / GUM SOOTHER, VARIOUS
FDA 510(k)
FDA Class 2
·Dental
CLEARGLIDE PRECISION BIPOLAR DEVICE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
POSSIS ANGIOJET X-STREAM RHEOLYTIC THROMBECTOMY CATHETER, MODEL 103587-002
FDA 510(k)
FDA Class 2
·Cardiovascular
BD NANO¿ ULTRA-FINE¿ PEN NEEDLES
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND CO.·Product code FMI·February 25, 2022
CLEARGLIDE EVH SMALL
FDA Adverse Event
Malfunction
·SORIN GROUP USA·Product code GEI·October 2, 2009
CLEARGLIDE EVH SMALL
FDA Adverse Event
Malfunction
·SORIN GROUP USA·Product code GEI·October 14, 2009
CLEARGLIDE EVH SMALL
FDA Adverse Event
Malfunction
·SORIN GROUP USA·Product code GEI·October 14, 2009
CLEARGLIDE EVH SMALL
FDA Adverse Event
Malfunction
·SORIN GROUP USA·Product code GEI·October 14, 2009
CLEARGLIDE EVH SMALL
FDA Adverse Event
Malfunction
·SORIN GROUP USA·Product code GEI·October 16, 2009
CLEARGLIDE EVH LONGVIEW W/SCIS
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code GEI·November 23, 2009
CLEARGLIDE EVH SMALL
FDA Adverse Event
Malfunction
·SORIN GROUP USA·Product code GEI·October 16, 2009
CLEARGLIDE EVH SMALL W/SCISSOR
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code GEI·October 16, 2009
CLEARGLIDE EVH LONGVIEW W/SCIS
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code GEI·November 9, 2009
UNICEL® DXI 800 ACCESS® IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·May 26, 2011
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·May 9, 2013
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code OYC·September 19, 2014
CLEARGLIDE EVH SMALL
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code GEI·November 24, 2009
CLEARGLIDE EVH SMALL W/SCISSOR
FDA Adverse Event
Malfunction
·SORIN GROUP USA, INC.·Product code GEI·November 3, 2009
BD NANO¿ ULTRA-FINE¿ PEN NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND CO.·Product code FMI·April 26, 2022