BEUDAMED
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    STERICHEK GLUTARALDEHYDE REAGENT STRIPS

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

    CD HORIZON® Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00885074036946·BONE SCREW 7040660 ILIAC 6.5X60 TI

    RAPONICEL™

    FDA UDI
    ADVANCED MEDICAL SOLUTIONS LIMITED·15032749040667·ACTIVHEAL® RAPONICEL™ ULTRA 2X46CM

    Pneumosure

    FDA UDI
    STRYKER CORPORATION·07613327055634·[High Flow Insufflator, Do not use if package ...

    HOMEPUMP, ECLIPSE, C-SERIES, PAINBUSTER, C-BLOC, ON-Q, EASYPUMP, ONE STEP KVO

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ESCORT II+ 400 SERIES (ESCORT PRISM), MODEL 20400, 20401, 20403, MONITOR, MODELS 20411, 20412, 20413

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TESS GLENOID REVERSE HEAD DIAMETER 36

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·October 27, 2016

    ETEST FLUCONAZOLE FL 256 WW S30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

    ETEST FLUCONAZOLE FL 256 WW S30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

    ETEST FLUCONAZOLE FL 256 WW S30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

    ETEST FLUCONAZOLE FL 256 WW S30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

    ETEST FLUCONAZOLE FL 256 WW S30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

    ETEST FLUCONAZOLE FL 256 WW S30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

    ETEST FLUCONAZOLE FL 256 WW S30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

    ETEST FLUCONAZOLE FL 256 WW S30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, SA·Product code NGZ·May 7, 2021

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·April 8, 2013

    COLLEAGUE 3 VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·May 9, 2008

    VITALITY

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·April 6, 2011

    PKG; HIGH FLOW II TUBESET FOR PNEUMO SURE (10-PK)

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code HIF·September 24, 2022

    Stryker High Flow II Tube Set, REF 0620-040-660, an accessory to the PNEUMO SURE High Flow Insufflator, Disposable, Rx, Sterile.

    FDA Recall
    Terminated ·Stryker Corporation·Product code HIF·March 7, 2019