BEUDAMED
    31 results · 22ms · Sources: EU EUDAMED, US FDA

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    LOQTEQ Distal Lateral Femur Plate 4.5 System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772777457·LUMBAMED PLUS FLEX PAD WM SILVER III

    10M - Southwest Gas Corp

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588010434·10M - Southwest Gas Corp

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07311K0100430·Caddie Lid, Adjustable Cross Links

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319744178·Tessier Periosteal Elevator 7" (17.5cm), 7mm wi...

    Best Seal

    FDA UDI
    BEST SEAL SURGICAL DRAPES·00869319000220·Litho Drape

    EXPLOR

    FDA UDI
    Biomet Orthopedics, LLC·00880304438330·

    Best Seal

    FDA UDI
    BEST SEAL SURGICAL DRAPES·06975424193994·Litho Drape

    CSM INTERNAL-R IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    Field Orthopaedics Bony Trauma Extremity System (BTES) Plate Range and Plate Screws; Field Orthopaedics Bony Trauma Extremity System (BTES) Screw Range

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FEP

    FDA UDI
    Merit Medical Systems, Inc.·00884450000625·

    EXPLOR 9X30MM IMPL STEM W/SCR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWI·September 20, 2018

    INDIGO SYSTEM ASPIRATION CATHETER 7D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code QEW·August 3, 2022

    VERSAPORT V2 RT 5MM OBTURATOR W/5MM SEAL

    FDA Adverse Event
    Malfunction ·PONCE-USS·Product code GCJ·October 21, 2008

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·August 12, 2011

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code LWS·July 8, 2013

    INDIGO SYSTEM ASPIRATION CATHETER 7D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code QEW·August 20, 2022

    EXPLOR 8X28MM IMPL STEM W/SCR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWI·October 7, 2020

    EXPLOR 9X30MM IMPL STEM W/SCREW

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWI·June 7, 2019

    EXPLOR 8X28MM IMPL STEM W/SCR

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWI·April 25, 2017