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

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    HUMID-VENT TRACH-VENT

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    Edge™ Diamond TMC012-8C Tapered Modified Chamfer

    FDA UDI
    CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172004763·Diamond dental bur, reusable

    DILATING TIP TROCAR WITH STABILITY SLEEVE - 12MM DIAMETER

    FDA Adverse Event
    Injury ·Product code GCJ·June 20, 2006

    Allied Biocompat Abutment for Nobel Replace Interface

    FDA 510(k)
    FDA Class 2 ·Dental

    B-CARE POWDERED LATEX EXAMINATION GLOVES

    FDA 510(k)

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·February 9, 2013

    INSIGNIA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·January 7, 2011

    DEXTRUS 4136

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVN·July 23, 2014

    MEDTRONIC LEAD

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code DXY·July 14, 2025