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

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    Filters Regulation: Us FDA ×

    VACUETTE MULTI-SAMPLE NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668109083·RANDOLPH CYCLODIALYSIS CANNULA STANDARD

    GUARDIAN HEMOSTASIS VALVE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Mag Vita TMS Therapy System w/Theta Burst Stimulation

    FDA 510(k)
    FDA Class 2 ·Neurology

    INFUSION DEVICES - UNKNOWN

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·September 19, 2024

    5.0MM TI LOCKING SCREW W/T25 STARDRIVE 70MM FOR IM NAILS

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·February 22, 2013

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 19, 2011

    ACCU-CHEK ® SPIRIT COMBO

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LZG·August 1, 2014