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

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    RADIONICS SIPHON LIMITING DEVICE (SLD)

    FDA 510(k)
    FDA Class 2 ·Neurology

    Needle Holder

    FDA UDI
    KATENA PRODUCTS, INC.·00841668108185·DREWS NEEDLE HOLDER STRAIGHT WITH LOCK

    Optima XR240amx

    FDA 510(k)
    FDA Class 2 ·Radiology

    CANCELLOUS SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC, INC.·Product code KWP·March 31, 2015

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·November 23, 2016

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·May 16, 2017

    6800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 23, 2014

    LIGASURE HS XTD DISP ELEC/CORD

    FDA Adverse Event
    Malfunction ·COVIDIEN LP·Product code GEI·January 23, 2013

    FREEDOM SELF CATH FEMALE CH14

    FDA Adverse Event
    Malfunction ·COLOPLAST MANUFACTURING US, LLC·Product code KOD·January 18, 2011

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·February 23, 2016

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·February 23, 2016

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·February 23, 2016

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·February 23, 2016

    TSRH SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·August 21, 2020

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·December 4, 2012

    BIOMET StageOne Knee Tibial Cement Spacer Mold, 65 MM, Silicone, Sterile, Item 433165.

    FDA Enforcement
    Class II ·Terminated·Biomet, Inc.·April 15, 2020