BEUDAMED
    11 results · 18ms · Sources: EU EUDAMED, US FDA

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    VASCULAR GRAFT PROST. OF EXPANDED PTFE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Rongeur

    FDA UDI
    KATENA PRODUCTS, INC.·00841668108529·BEYER RONGEUR SINGLE ACTION

    Curiteva Pedicle Screw System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PRESSURE TUBING

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 6, 2014

    ACCESS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FPA·October 15, 2012

    ENTRUST AT

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code LWS·August 10, 2010

    DRILL BIT Ø4.3 L280 F/324.007

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HTW·July 11, 2023

    25MM VERSA-DIAL TAPER ADAPTOR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·June 12, 2023

    BEARING +3 MM RETENTIVE THICKNESS 36 MM DIAMETER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·June 8, 2023

    COMP RVRS 25MM BSPLT HA+ADPTR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·June 12, 2023