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

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    CENTRIMED SYSTEM 1 W/24 VOLT BATTERY POWER SUPPLY

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Arch Lock

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746146749·ARCH STOP WELDABLE 1.25MM 018X025 100/PKG

    Sklar

    FDA UDI
    SKLAR CORPORATION·10649111066276·OTIS BOUGIE A BOULE 14FR

    Stainless Steel Surgical Kits

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PRIMACONNEX INTERNAL CONNECTION IMPLANT SYSTEM, PRIMACONNEX INTERNAL CONNECTION PROSTHETICS

    FDA 510(k)
    FDA Class 2 ·Dental

    TITAN OTR

    FDA Adverse Event
    Injury ·COLOPLAST A/S·Product code FHW·April 26, 2022

    IVT DISPOSABLE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - AIBONITO·Product code KPE·June 5, 2014

    CONTAK RENEWAL

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·October 4, 2010

    PROSTHESIS INTERVERTEBRAL DISC

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code MJO·June 17, 2015