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

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    BOBCAT DX

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970543·anteriors; shade BL3; mould UCS

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111338830·JOHNSON TUCKER HOOK &FORK 6.5"

    VIPER PRIME™ Screws with Fenestrations

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODIFICATION TO HEALTH BUDDY APPLIANCE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SEE H10

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code NBC·April 18, 2013

    TENACULUM FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·February 20, 2013

    32MM MOD HEAD COCR -6MM NECK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·July 31, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Injury ·LIFESCAN INC.·Product code NBW·January 25, 2011

    CERAMIC ELECTRODE TIP L-HK F/GK372R

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code GEI·July 5, 2019

    InterGard Knitted Collagen Coated Vascular prostheses marketed under 510(k) # K964625; InterGard Woven Collagen Coated Vascular prostheses marketed under 510(k} #K970843 and K984294.

    FDA Recall
    Terminated ·Intervascular S.A.S. Zone Industrielle Athelia I La Ciotat Cedex France·Product code DSY·December 9, 2009