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

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    QUANTEC-E IRRIGATION SYSTEM

    FDA 510(k)
    FDA Class 1 ·Dental

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517405050·CoRoent® XLT, 10x16x35mm

    Gen. Acces/ Instr. Tip Guard

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112281·SURG-I-BAND GREY

    ZAVATION

    FDA UDI
    Zavation LLC·00842166175051·Rod Persuader

    TAUB - Trident - IMPULSE

    FDA UDI
    Taub Products·D8379910350·IMPULSE is a hand held and operated crown remov...

    FULL BREATH SLEEP APPLIANCE LOWER (FBSL)

    FDA 510(k)
    FDA Class 2 ·Dental

    FETASONDE FETAL ACTIVITY MONITOR

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    COLORADO 2 SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC INC.·Product code MNH·December 4, 2009

    COLORADO II SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code MNH·May 19, 2017

    COLORADO SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·October 17, 2016

    PULSE GEN MODEL 103

    FDA Adverse Event
    Malfunction ·LIVANOVA USA, INC.·Product code LYJ·March 6, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 15, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014

    COLORADO II SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC.·Product code KWP·July 26, 2011