BEUDAMED
    59 results · 22ms · Sources: EU EUDAMED, US FDA

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    AQUAMANTYS 3 PUMP GENERATOR, BIPOLAR SEALER, BIPOLAR SEALER WITH CUTTING

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517635976·CoRoent Ant TLIF PEEK, 11x11x28mm 15°

    AOS TIBIAL NAIL 11mm x 28.5cm

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665016192·

    Surgical Instrument

    FDA UDI
    Jeil Medical Corporation·08806390880732·

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111119408·UTILITY SCISS 7 1/2" PURPLE

    Summa Orthopaedics System Surgical Instrument

    FDA UDI
    Jeil Medical Corporation·08800089402717·

    NEPHROS DSU FILTER, NEPHROS MSU FILTER, NEPHROS SSU FILTER

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

    CONSTELLATION VISION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    BD LUER-LOK¿ TIP SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·October 11, 2022

    BD BACTEC¿ MGIT¿ 960 SIRE KIT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·June 13, 2023

    BD LUER-LOK¿ 10 ML BULK PACK LUER LOCK TIP WITHOUT SAFETY

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·February 18, 2022

    HEARTMATE II LVAD

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·May 9, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·September 23, 2014

    ZOOM CRITICAL CARE BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·May 18, 2011

    CADD SOLIS VIP PUMPS

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FRN·June 3, 2022

    CADD-SOLIS VIP AMBULATORY INFUSION PUMP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FRN·August 18, 2022

    BD BACTEC¿ MGIT¿ 960 SIRE KIT

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code MJA·August 7, 2025

    BD BACTEC¿ MGIT¿ 960 SIRE KIT

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code MJA·August 7, 2025

    BD BACTEC¿ MGIT¿ 960 SIRE KIT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code MJA·August 8, 2025

    BD BACTEC¿ MGIT¿ 960 SIRE KIT

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code MJA·August 8, 2025