BEUDAMED
    15 results · 20ms · Sources: EU EUDAMED, US FDA

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    MEDLINES REPEAT PERFORMANCE SURGICAL PACK SYSTEM

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

    STABILITY

    FDA UDI
    Stryker GmbH·00886385022598·uHead Head Trial, Size 4

    CHLORAPREP ONE STEP

    FDA Adverse Event
    Malfunction ·CAREFUSION 213, LLC 0113·Product code KXG·December 13, 2021

    RIWOtrack Navigation System

    FDA 510(k)
    FDA Class 2 ·Neurology

    CERALAS D 10-60 810NM LASER SYSTEM WITH ENDO LASER VEIN SYSTEM KIT

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

    CHLORAPREP ONE STEP FREPP

    FDA Adverse Event
    Malfunction ·CAREFUSION 213, LLC 0113·Product code KXF·May 26, 2021

    CHLORAPREP ONE STEP

    FDA Adverse Event
    Malfunction ·CAREFUSION 213, LLC 0113·Product code KXF·August 18, 2021

    CHLORAPREP ONE STEP

    FDA Adverse Event
    Malfunction ·CAREFUSION 213, LLC 0113·Product code KXF·August 18, 2021

    CHLORAPREP ONE STEP

    FDA Adverse Event
    Malfunction ·CAREFUSION 213, LLC 0113·Product code KXG·August 18, 2021

    Compress Device Segmental Anchor Plug, 22 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178412

    FDA Enforcement
    Class II ·Ongoing·Biomet, Inc.·November 29, 2023

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 28, 2013

    SUPERA BILIARY STENT DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·IDEV TECHNOLOGIES, INC.·Product code FGE·December 14, 2010

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·July 12, 2014

    CHLORAPREP ONE STEP

    FDA Adverse Event
    Injury ·CAREFUSION 213, LLC 0113·Product code KXG·February 15, 2022

    HA Pins (DFS HA Cort Screw), Hoffman/Colles Pins (Colles CSER Sterile w/ Pin Kit) Item Nos: HAA60-09030 HAA60-09040 HAA60-10030 HAA60-10040 HAA60-11030 HAA60-11040 HAA60-11050 HAA60-12040 HAA60-12060 HAA60-13030 HAA60-13040 HAA60-13050 HAA60-13060 HAA60-13070 HAA60-14050 HAA60-14080 HAA60-14090 HAA60-15020 HAA60-15030 HAA60-15040 HAA60-15050 HAA60-15060 HAA60-16030 HAA60-16040 HAA60-16050 HAA60-16070 HAA60-16090 HAA60-17040 HAA60-17060 HAA60-17080 HAA60-18010 HAA60-18030 HAA60-18040 HAA60-18050 HAA60-18060 HAA60-18090 HAA60-20030 HAA60-20040 HAA60-20050 HAA60-20060 HAA60-20080 HAA60-20090 HAA60-22050 HAA60-22060 HAA60-25030 HAA60-25040 HAA60-25050 HAA60-25060 HAA60-30060 HAB60-09030 HAB60-10030 HAB60-10040 HAB60-11040 HAB60-11050 HAB60-12040 HAB60-12060 HAB60-13040 HAB60-13050 HAB60-13060 HAB60-14050 HAB60-15060 HAB60-16070 HAB60-16090 HAB60-17080 HAB60-18010 HAB60-18090 HAB60-20080 HAB60-20090 808200000 Product Usage: These devices are intended for osteosynthesis, external fixation of fractures or bone lengthening procedures.

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·December 4, 2019