BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    DUAFIT INTERGPHALANGEAL IMPLANT, PEEK-FUSE INTERPHALANGEAL IMPLANT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DIGITAL THERMOMETER (WITH DISPOSABLE THERMOMETER COVER)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    INTERLOCK FIBERED IDC OCCLUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 29, 2025

    VA LOCKSCR Ø2.4 SELF-TAP L16 TAN

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWC·May 29, 2013

    TALENT TAA

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR·Product code MIH·October 1, 2014

    MINICAP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·June 17, 2011

    Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564, CD3255-40/100038224, CD3255-40Q/100036514

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018