BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    DALE COMBO TRACHEOSTOMY TUBE HOLDER

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    ERA® Implant Abutment Micro Ang. Base, 4mm Cuff (AX)

    FDA UDI
    STERNGOLD DENTAL LLC·00841549103780·Implant retained overdentures are an establishe...

    GIZA(R) VERTEBRAL BODY REPLACEMENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SURESET INFUSION SET, MODEL 8023

    FDA 510(k)
    FDA Class 2 ·General Hospital

    O3 PEDIATRIC SENSOR

    FDA Adverse Event
    Malfunction ·MASIMO - 15750 ALTON PKWY·Product code MUD·August 20, 2022

    O3 PEDIATRIC SENSOR

    FDA Adverse Event
    Malfunction ·MASIMO - 15750 ALTON PKWY·Product code MUD·August 19, 2022

    LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code LDD·May 15, 2014

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012

    DUR MAR NEUT LINER 28IDX58OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·August 16, 2010