BEUDAMED
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    ANGIOJET SOLENT PROXI THROMBECTOMY SET MODEL 109676-001

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·00636257010068·M.3 SOFT OA BRACE, VARUS, LEFT, 2X

    Bur PM2-70 80K Mstick Ø4.0 St

    FDA UDI
    Bien-Air Surgery SA·17630055519969·

    ARGELOY NP V (1 ao)

    FDA UDI
    ARGEN CORPORATION, THE·D818101406·Base metal alloy

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383556040·Gutta Percha Points is used to root canal filin...

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383500821·Gutta Percha Points is used to root canal filin...

    Admiral

    FDA UDI
    Seaspine Orthopedics Corporation·10889981277192·Modular Trial, 14 x 13 x 6mm, 7 Deg Lordosis

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M93051014061T10·Toothed Curette Custom Ang #6, 5" Silicone Handle

    HA/GOLD TOTAL AND PARTIAL, REGULAR AND OFFSET, OSSICULAR REPLACEMENT PROSTHESES

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    SPINAL MESH SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Ascendant

    FDA UDI
    Choice Spine, LP·10885862260475·

    PYRAMESH C TITANIUM MESH

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC.·Product code EZX·August 12, 2011

    PYRAMESH

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code EZX·September 29, 2015

    ASTERX EXPANDABLE CORPECTOMY SYSTEM

    FDA Adverse Event
    Injury ·MSD DEGGENDORF MFG·Product code MQP·March 4, 2019

    ASTERX EXPANDABLE CORPECTOMY SYSTEM

    FDA Adverse Event
    Injury ·MSD DEGGENDORF MFG·Product code MQP·March 4, 2019

    ELECTRONIC GAS BLENDER

    FDA Adverse Event
    Malfunction ·LIVANOVA DEUTSCHLAND·Product code DTX·November 19, 2025

    PYRAMESH C TITANIUM MESH

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code EZX·October 26, 2019

    STOCKERT S3 GAS BLENDER

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·December 22, 2014

    RA CATH KIT: 20 GA X 1-3/4IN

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code DQX·May 3, 2013

    MINICAP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·May 24, 2011