BEUDAMED
    53 results · 25ms · Sources: EU EUDAMED, US FDA

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    FDA 510(k)
    FDA Class 2 ·Radiology

    Trial Cups

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215038977·

    PROVU (TM) DENTAL X-RAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    STARDUST II

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MINIMARK DENTAL IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·ACE SURGICAL SUPPLY CO.·Product code DZE·June 5, 2013

    SYMBIQ SINGLE CHANNE

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·October 6, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 22, 2011

    SENRI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·April 2, 2021

    GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DYB·February 21, 2018

    SENRI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 9, 2019

    SENRI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 11, 2024

    SENRI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·February 20, 2020

    SENRI

    FDA Adverse Event
    Injury ·KANEKA·Product code LIT·March 12, 2019

    SENRI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·May 6, 2025

    SENRI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·December 24, 2025

    DIVA

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 7, 2020

    DIVA

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 7, 2020

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 12, 2020

    18 SHIDEN HP

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 19, 2025

    SENRI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 12, 2025