BEUDAMED
    10 results · 24ms · Sources: EU EUDAMED, US FDA

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    Pixx2430 Digital Diagnostic X-Ray Receptor Panel

    FDA 510(k)
    FDA Class 2 ·Radiology

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319741733·Spinal Fusion Curette 7-3/4" (20cm), reverse an...

    OMNI V SBRT POSITIONING SYSTEM, MODEL RT-4500

    FDA 510(k)
    FDA Class 2 ·Radiology

    POWDER-FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CB-X II DUAL-ENDED CLEANING BRUSH

    FDA Adverse Event
    Malfunction ·AVENT S. DE R.L. DE C.V.·Product code FEB·October 3, 2008

    PROSTAR XL SUTURE-MEDIATED CLOSURE

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·June 26, 2013

    SITTER II

    FDA Adverse Event
    Malfunction ·J. T. POSEY CO.·Product code KMI·July 29, 2011

    INSPIRE 7M HOLLOW FIBER OXYGENATOR, INSPIRE 7 DUAL HOLLOW FIBER OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·June 14, 2019

    MEDTRONIC ICD

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code DXY·March 31, 2020

    INSPIRE 7M HOLLOW FIBER OXYGENATOR, INSPIRE 7 DUAL HOLLOW FIBER OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·June 19, 2019