BEUDAMED
    8 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    SYBRON/KERR CONTOUR

    FDA 510(k)
    FDA Class 2 ·Dental

    StealthFix Intraosseous Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LUFUCON SILVER ALGINATE DRESSING 50X50MM, LUFUCON SILVER ALGINATE DRESSING 100X100MM, LUFUCON SILVER DRESSING 200X100MM

    FDA 510(k)
    FDA Unclassified ·Unknown

    UNKNOWN PROTACK

    FDA Adverse Event
    Injury ·US SURGICAL PUERTO RICO·Product code GDW·June 26, 2019

    UNKNOWN PARIETEX

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION SAS·Product code FTL·June 26, 2019

    NATURALYTE

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·May 9, 2014

    ULTRACISION HARMONIC SCALPEL HAND PIECE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code LFL·October 30, 2007

    FENTA

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·November 2, 2012