BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    DISP. TOOTHBRUSH W/3 G. TUBE OF TOOTHPST

    FDA 510(k)
    FDA Class 1 ·Dental

    C100 WRINKLE REDUCTION DEVICE

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

    MODIFICATION TO VASCULAR CLOSURE DEVICE

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

    TELESCOPE, 10 MM, 0°, QUICK LOCK, AUTOCLAVABLE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HET·October 31, 2023

    TELESCOPE, 10 MM, 30°, HD, QUICK LOCK, AUTOCLAVABLE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code EWY·June 5, 2023

    ACCESS® 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code JJE·May 15, 2014

    EXTERNAL PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA INC.·Product code DTE·October 31, 2012

    GENTLEPOWER LUX CONRA ANGLE 25LPA

    FDA Adverse Event
    Injury ·KAVO DENTAL GMBH·Product code EFB·August 16, 2010