BEUDAMED
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    MEDTRONIC SINGLE USE ESOPHAGEAL MANOMETRIC CATHETER, MEDTRONIC SINGLE USE ANORECTAL MANOMETRIC CATHETER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·H65810321381·ZODIAC GLOVE PF LATEX

    ZODIAC

    FDA UDI
    HENRY SCHEIN, INC.·00304040056950·ZODIAC X-Small

    Baltic Denture System BDCreator

    FDA UDI
    Merz Dental GmbH·D7091032138·Baltic Denture System BDCreator PLUS

    BUSCH®, BNA®

    FDA UDI
    BUSCH & CO. GmbH & Co. KG·D8120321381·Diamond, cone rounded edge, COOL DIAMANT, mediu...

    SlimLine®

    FDA UDI
    ZIMMER SPINE, INC.·00889024403901·

    PARADIGM SILHOUETTE, MODELS MMT-377, 378, 379, 380

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MODIFICATION TO ACIS (AUTOMATED CELLULAR IMAGING SYSTEM)

    FDA 510(k)
    FDA Class 2 ·Hematology

    COAPTITE INJECTABLE IMPLANT

    FDA Adverse Event
    Other ·MERZ NORTH AMERICA, INC·Product code LNM·October 17, 2013

    COAPTITE INJECTABLE IMPLANT

    FDA Adverse Event
    Other ·MERZ NORTH AMERICA, INC·Product code LNM·October 17, 2013

    JTS UNIT

    FDA Adverse Event
    Malfunction ·STANMORE IMPLANTS WORLDWIDE·Product code KRO·September 11, 2018

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·March 6, 2013

    CARPENTIER-EDWARDS PERIMOUNT MAGNA MITRAL EASE PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·March 28, 2011

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR - REDWOOD CITY·Product code MGB·April 18, 2008

    JTS COIL

    FDA Adverse Event
    Malfunction ·STANMORE IMPLANTS WORLDWIDE·Product code KRO·February 13, 2020

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 12, 2026

    COAPTITE INJECTABLE IMPLANT

    FDA Adverse Event
    Injury ·MERZ NORTH AMERICA, INC.·Product code LNM·October 29, 2015

    COAPTITE INJECTABLE IMPLANT

    FDA Adverse Event
    Injury ·MERZ NORTH AMERICA, INC.·Product code LNM·October 29, 2015

    COAPTITE INJECTABLE IMPLANT

    FDA Adverse Event
    Other ·MERZ NORTH AMERICA, INC.·Product code LNM·October 29, 2014

    PANEL PHOENIX PMIC-110

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026