BEUDAMED
    26 results · 29ms · 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.

    CLEARGLIDE PRECISION BIPOLAR DEVICE

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

    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

    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

    KALORE™

    FDA UDI
    Gc America Inc.·D0470035871·KALORE™ Syringes (2 mL/4 g) D2

    KALORE™

    FDA UDI
    Gc America Inc.·14548161293211·KALORE™ Syringes (2 mL/4 g) D2

    SP5-1U Ultrasonic Probe(FDA)

    FDA UDI
    Shenzhen Mindray Bio-Medical Electronics Co., Ltd.·06944904088426·

    19 GA PLASTIC REINFORCED EPIDURAL CATHETER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SHUTTLE STOP

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

    DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code PQF·August 15, 2018

    9800 FLUOROTRAK, IT3500 SPINE

    FDA Adverse Event
    Malfunction ·GE HEALTHCARE·Product code JAA·November 30, 2005