BEUDAMED
    8 results · 29ms · Sources: EU EUDAMED, US FDA

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    K-Y Silicone

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ORTHO SUMMIT SAMPLE HANDLING SYSTEM

    FDA Adverse Event
    Malfunction ·HAMITON BONADUZ AG·Product code JTC·May 16, 2000

    DEKA SMARTXIDE AND DELIVERY ACCESSORIES

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

    GETINGE 400HC/500HC SERIES STEAM STERILIZER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    LAP-BAND AP ADJUSTABLE GASTRIC BANDING SYSTEM (STANDARD)

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·October 10, 2014

    ACCESS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MALTA·Product code FPA·July 23, 2011

    VERSAPORT V2 BLADELESS OPT 12

    FDA Adverse Event
    Malfunction ·COVIDIEN LP, FORMERLY REGISTERED AS UNITED STATES·Product code GCJ·June 12, 2013

    PINNACLE SECTOR II CUP 60MM

    FDA Adverse Event
    Injury ·. DEPUY ORTHOPAEDIC INC, 1818910·Product code KWA·May 25, 2018