BEUDAMED
    12 results · 18ms · Sources: EU EUDAMED, US FDA

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    ACS GENTAMICIN

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    BASE

    FDA UDI
    Nuvasive, Inc.·00887517701152·BASE Ti HL Implant, 10x42x30mm 20°

    Spinous Process System

    FDA UDI
    Seaspine Orthopedics Corporation·10889981096199·Inserter, Spinous Process Spacer

    iNSitu™ Hip System

    FDA UDI
    NEXTSTEP ARTHROPEDIX, LLC·00816127023293·U-Joint Stem Extractor

    TNL-ULTRA ASSAY FOR THE ADVIA CENTAUR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Strauss Surgical Resection Instruments

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ADVIA CENTAUR CKMB AND TROPONIN ULTRA ASSAY

    FDA Adverse Event
    Other ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JHX·July 29, 2010

    DEFIBRILLATOR, AUTOMATIC IMPLANTABLE CARDIOVERTER

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·February 9, 2013

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·July 23, 2014

    ACCU-CHEK ® AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·January 7, 2011

    REF H10

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code MMI·August 9, 2016

    ATELLICA IM HIGH-SENSITIVITY TROPONIN I (TNIH)

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code MMI·December 10, 2020