BEUDAMED
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    HexaPLUS S OneDrill Implant System

    FDA UDI
    OSSEOFUSE INTERNATIONAL, INC.·00810044843033·

    LineLogic™

    FDA UDI
    SMD Manufacturing LLC·00851780008201·Sterile, Linelogic™ 8.5 Fr Catheter Stabilizati...

    LineLogic™

    FDA UDI
    SMD Manufacturing LLC·00851780008102·Sterile, Linelogic™ 7 Fr Catheter Stabilization...

    LineLogic™

    FDA UDI
    SMD Manufacturing LLC·00851780008003·Sterile, Linelogic™ 6 Fr Catheter Stabilization...

    Tuohy Borst 9 FR (11G) LLM

    FDA UDI
    Promepla·03700512961949·

    Tuohy Borst 9 FR (11G) LLM

    FDA UDI
    Promepla·03700512965480·

    ACCUCHEK LLM

    FDA Adverse Event
    Injury ·BOEHRINGER MANNHEIM CORP·Product code CFR·April 4, 1997

    ACCUCHEK LLM

    FDA Adverse Event
    Injury ·BOEHRINGER MANNHEIM CORP.·Product code CFR·April 4, 1997

    SYRINGE 10ML LL BNS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·November 6, 2019

    MAMMOMAT REVELATION

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE GMBH·Product code MUE·June 24, 2022

    UNK MAMMARY IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FWM·January 17, 2024

    VIDEO TELESCOPE "ENDOEYE", 10 MM, 30°, PAL, HD COMPATIBLE, AUTOCLAVABLE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code NWB·December 6, 2024

    FS MIS UNI FEM COMP L LM/RL

    FDA Adverse Event
    Injury ·STRYKER HOWMEDICA OSTEONICS·Product code HSX·March 1, 2001

    SYRINGE NON STERILE 50ML LL

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·January 18, 2024

    PROXIMALE - 28 CM (11") SMALLBORE EXT SET W/6-PORT NANOCLAVE® MANIFOLD, CHECK VA

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FMG·December 8, 2022

    BD PHASEAL ADMINISTRATION PRODUCTS - IV BAG ACCESS

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·May 3, 2021

    CANNULA & CATHETER

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DWF·June 17, 2021

    TUBING SETS

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DWE·August 8, 2024

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·May 1, 2026

    TUBING SET

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DWF·August 3, 2022