BEUDAMED
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    GN ReSound

    FDA UDI
    Gn Hearing A/S·05708296126378·HI,RS VOT950-DWE ITE

    GN ReSound

    FDA UDI
    Gn Hearing A/S·05708296126361·HI,RS VOT930-DWE ITC

    GN ReSound

    FDA UDI
    Gn Hearing A/S·05708296078370·HI,RS LT9ITC-DWE-MP

    GN ReSound

    FDA UDI
    Gn Hearing A/S·05708296129089·HI,RS LS9ITC-DWE-MP

    UNKNOWN ZIMMER ARTICULAR SURFACE

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code JWH·July 3, 2007

    TRIDENT 0 DEG X3 INSERT 32MM HEAD

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·June 16, 2014

    SPECTRATHERM

    FDA Adverse Event
    Other ·GAMBRO·Product code BRZ·May 10, 2007

    AFFINITY CP CENTRIFUGAL PUMP

    FDA Adverse Event
    Injury ·PERFUSION SYSTEMS·Product code DWE·June 8, 2018

    COGNIS 100-D

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CARDIOVASCULAR DIVISION·Product code NIK·August 25, 2009

    ITREVIA 7 HF-T QP DF4 IS4

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NIK·December 9, 2016

    REAGENT RED BLOOD CELLS BIOTESTCELL 3

    FDA Adverse Event
    Malfunction ·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code LKJ·August 30, 2011

    DAYTON LINEAR ACTUATOR

    FDA Adverse Event
    Malfunction ·MIDMARK CORPORATION SUPLLIED; DAYTON ELECTRIC MFG. CO.·November 17, 1992

    AFFINITY CP CENTRIFUGAL PUMP

    FDA Adverse Event
    Injury ·PERFUSION SYSTEMS·Product code DWE·June 8, 2018

    COBALT¿ HF QUAD CRT-D MRI SURESCAN¿

    FDA Adverse Event
    Injury ·MEDTRONIC EUROPE SARL·Product code NIK·October 16, 2025

    BLOOD GROUPING REAGENT IH-CARD ABO/D(DVI-)+REV A1,B

    FDA Adverse Event
    Malfunction ·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code QHR·March 6, 2025

    LIBERTY CYCLER SET, SINGLE CONN./EXT. DL

    FDA Adverse Event
    Injury ·ERIKA DE REYNOSA, S.A. DE C.V.·Product code FKX·August 12, 2025

    CT LUCIA

    FDA Adverse Event
    Injury ·CARL ZEISS MEDITEC PRODUCTION LLC·Product code HQL·September 24, 2025

    EVIS LUCERA PLEURA VIDEOSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code EWY·August 12, 2022

    EVIS PLEURA VIDEOSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code EWY·August 12, 2022

    ENDURANT II

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·May 4, 2015