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

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    Filters Regulation: Us FDA ×

    PRO-TEC DISPOSBLE SHARPS CONTAINERS Q1

    FDA 510(k)
    FDA Class 2 ·General Hospital

    N/A

    FDA UDI
    Tyber Medical, LLC·M695M9452750·

    OSTEONICS(R) MPSS HIP STEM SERIES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SOFT DENTURE RELINE MATERIAL ELASTOLINE

    FDA 510(k)
    FDA Class 2 ·Dental

    HEARTSTART XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 6, 2014

    DRILL BIT Ø2/1.15 CANN L150/48 3FLUTE

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTW·February 6, 2013

    90018107 LAP SPG P-W 18X18 NON-STR

    FDA Adverse Event
    Malfunction ·GRAND MEDICAL·Product code EFQ·December 21, 2010

    EVOLUT FX DCS

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NPT·September 8, 2025