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

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    SUCTION GUILLOTINE DEVICE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981194574·Interbody, 9mm x 32mm x 14mm, 20 deg

    Reef TH

    FDA UDI
    Seaspine Orthopedics Corporation·10889981202569·Interbody, 9mm x 32mm x 14mm, 20 deg

    DATACAPTOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NERIA SOFT 90 INFUSION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    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

    RUNWAY GUIDE CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQY·May 8, 2013

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 3, 2014

    PENTA

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·January 25, 2013

    FIRST PICC

    FDA Adverse Event
    Malfunction ·ARGON MEDICAL DEVICES, INC.·Product code FOZ·December 14, 2010