BEUDAMED
    7 results · 37ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    AN85/AN86 EO Indicators

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DYNA-EXTOR II

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SILHOUETTE, MODEL 1000.01

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    PRODIGY AUTOCODE

    FDA Adverse Event
    Injury ·OK BIOTECH CO., LTD.·Product code NBW·March 29, 2018

    530G INSULIN PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·October 14, 2014

    ECHELON* 60 ENDOPATH**

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 20, 2011

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·May 24, 2013