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

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    CORNING TRANSPHOR

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    UNASSIGNED

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BOUCHER DEGROOT HEAD POSITIONING GLASSES, MODEL 8080

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·May 8, 1998

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·May 8, 1998

    AESPIRE 7900

    FDA Adverse Event
    Malfunction ·DATEX-OHMEDA·Product code BSZ·February 11, 2014

    ABSOLUTE PRO VASCULAR SELF-EXPANDING STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIO·October 22, 2012

    STARCLOSE SE VASCULAR CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR - REDWOOD CITY·Product code MGB·August 12, 2010

    BD PLATE CAMPYLOBACTER SB 100MM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON DE MEXICO·Product code JSJ·June 2, 2022

    Nova - EZ CHEM Linearity Solution P/N 9618, Nova Biomedical, Waltham, MA 02454

    FDA Recall
    Terminated ·Nova Biomedical Corporation·Product code CGL·November 2, 2007

    Nova - EZ CHEM Control Solution P/N 9612, Nova Biomedical, Waltham, MA 02454

    FDA Recall
    Terminated ·Nova Biomedical Corporation·Product code CGL·November 2, 2007

    Nova - EZ CHEM Creatinine Meter: SRS Versions 5.1 and 5.2 P/N 9600, Nova Biomedical, Waltham, MA 02454

    FDA Recall
    Terminated ·Nova Biomedical Corporation·Product code CGL·November 2, 2007

    Abbott Amplatzer Steerable Delivery Sheath (ASDS), REF ASDS-14F-075, is a percutaneous catheter (cardiac).

    FDA Recall
    Open, Classified ·Abbott·Product code DQY·June 12, 2023

    Amplatzer TorqVue LP Catheter (TVLPC), Model no. 9-TVLPC4F90/080

    FDA Recall
    Open, Classified ·Abbott·Product code DQY·March 17, 2025

    Amplatzer TorqVue LP Delivery System (TVLP), Model nos. 9-TVLP4F90/060 and 9-TVLP4F90/080

    FDA Recall
    Open, Classified ·Abbott·Product code DQY·March 17, 2025

    Abbot Navitor, Vision Technology, Transcatheter Aortic Heart Valve, 29 mm, NVRO-29, Sterile

    FDA Recall
    Open, Classified ·Abbott Medical·Product code NPT·October 17, 2024

    Abbott Navitor Transcatheter Aortic Heart Valve, 27 mm, NVTR-27, Sterile

    FDA Recall
    Open, Classified ·Abbott Medical·Product code NPT·October 17, 2024

    Abbott Navitor Transcatheter Aortic Heart Valve, 29 mm, NVTR-29, Sterile

    FDA Recall
    Open, Classified ·Abbott Medical·Product code NPT·October 17, 2024

    Abbott Navitor, Vision Technology, Transcatheter Aortic Heart Valve, 27 mm, NVRO-27, Sterile

    FDA Recall
    Open, Classified ·Abbott Medical·Product code NPT·October 17, 2024

    Abbott Navitor Titan, Vision Technology, Transcatheter Aortic Heart Valve, 35 mm, NVRO-35, Sterile

    FDA Recall
    Open, Classified ·Abbott Medical·Product code NPT·October 17, 2024