BEUDAMED
    27 results · 22ms · Sources: EU EUDAMED, US FDA

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    LEVEL 1 SNUGGLE WARM PEDIATRIC AND LARGE PEDIATRIC UNDERBODY BLANKET

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    iDMS Data Management System

    FDA UDI
    ACCURAY INCORPORATED·M65810615130·Software, Version 2.0, iDMS Data Management Sys...

    MI Product Line

    FDA UDI
    Medical Illumination International Inc.·00816835020003·MI-1000 Minor Surgical Light, Floor Stand

    SCOTT'S SELECT ALLOY 500/jar 2 SPILL

    FDA UDI
    SCOTT'S DENTAL SUPPLY L.L.C.·D77810615130·

    Tiche PTA Balloon Dilatation Catheter

    FDA UDI
    BrosMed Medical Co.,Ltd.·06958481477382·

    VISION LED

    FDA UDI
    Avante·00815871021654·DRE Vision LED, FLOOR MODEL

    MI Product Line

    FDA UDI
    Medical Illumination International Inc.·00816835020560·MI-1000 Minor Surgical Light, Floor Stand

    Zavation

    FDA UDI
    Zavation LLC·00842166170421·Cervical Interbody, 6 deg, 15mm x 13mm - 10mm

    Zavation

    FDA UDI
    Zavation LLC·00842166170384·Cervical Interbody, 6 deg, 15mm x 13mm - 6mm

    VISION LED

    FDA UDI
    Avante·00815871021692·DRE Vision LED, FLOOR MODEL

    Zavation

    FDA UDI
    Zavation LLC·00842166170414·Cervical Interbody, 6 deg, 15mm x 13mm - 9mm

    Zavation

    FDA UDI
    Zavation LLC·00842166170438·Cervical Interbody, 6 deg, 15mm x 13mm - 11mm

    Zavation

    FDA UDI
    Zavation LLC·00842166170445·Cervical Interbody, 6 deg, 15mm x 13mm - 12mm

    Zavation

    FDA UDI
    Zavation LLC·00842166170391·Cervical Interbody, 6 deg, 15mm x 13mm - 7mm

    Zavation

    FDA UDI
    Zavation LLC·00842166170407·Cervical Interbody, 6 deg, 15mm x 13mm - 8mm

    ACCU-CHEK ADVANTAGE MODULE

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    MP3U, POWER WHEELCHAIR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    AN UNSPECIFIED CLOSED SYSTEM ART LINE TRANSUDUCER

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code DRS·March 18, 2025

    UNSPECIFIED SAFESET TRANSPAC SETS

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code DRS·January 2, 2025

    UNSPECIFIED CENTRAL LINE TRANSDUCER SET

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code DRS·November 5, 2024