BEUDAMED
    22 results · 25ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    DERMAPAL WITH DIGITAL TIMER

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    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

    INFINION CX

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 8, 2024

    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

    IMUFLEX DISPOSABLES

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION/TERUMO BCT·Product code KSR·April 23, 2013

    RIATA ST ACTIVE FIXATION LEAD

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·July 11, 2008

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·April 27, 2011

    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

    CLEARGLIDE EVH SMALL

    FDA Adverse Event
    Malfunction ·SORIN GROUP USA·Product code GEI·October 16, 2009

    BIOLOX OPTION, HEAD, S, 44/-3.0, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·December 12, 2018