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

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    NanoKnife Generator (H78720300301US0); NanoKnife Single Electrode Activation Probe, 15 cm (H787204001090); NanoKnife Single Electrode Activation Probe, 25 cm (H787204001100); NanoKnife Single Electrode Probe Spacer (H787204003010)

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

    ENZYGNOST F+2 (MONOCLONAL) TEST KIT

    FDA 510(k)
    FDA Class 2 ·Hematology

    Pulse Oximeter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·November 11, 2014

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·September 10, 2011

    SELOX ST 53

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVN·July 23, 2013

    Model Number L111, ESSENTIO DR SL MRI Pacemaker

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025