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

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    E.Z. TEMEP, TEMPORARY FILLING MATERIAL

    FDA 510(k)
    FDA Class 2 ·Dental

    Reef TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981239916·Interbody, 9mm x 24mm x 13mm, 22 Deg

    Reef TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981240325·Trial, 9mm x 24mm x 13mm, 22 Deg

    WILTEK ELECTROCAUTERY ACTIVE CORD

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    CHROMOPHARE X 65

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·January 22, 2013

    ATTAIN STARFIX

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 14, 2010

    TENDRIL SDX

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 9, 2014

    LIGACLIP ENDOSCOPIC ROTATING MCA

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·June 6, 2017

    Presource PBDS, Shoulder Procedure, Kit, Circulator

    FDA Enforcement
    Class I ·Terminated·Cardinal Health, Medical Products & Services·May 15, 2013