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

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    Acetabular Dome Hole Plug

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    K-Systems

    FDA UDI
    Coopersurgical, Inc.·00888937025033·G95 Mini Incubator

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613113766·Adson Brown Tissue Forceps, 7 x 7 Teeth, Overal...

    Navbit Sprint System- Supine Registration, Navbit Sprint Kit - Lateral Registration

    FDA 510(k)
    FDA Class 2 ·Neurology

    AHL GENERIC GLASS IONOMER AESTHETIC RESTORATIVE

    FDA 510(k)
    FDA Class 2 ·Dental

    INRATIO

    FDA Adverse Event
    Malfunction ·BIOSITE INCORPORATED·Product code JPA·March 2, 2010

    GLIDEWELL HT IMPLANT Ø3.5 X 13 MM

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·October 28, 2025

    GLIDEWELL HT IMPLANT Ø3.5 X 13 MM

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC·Product code DZE·December 24, 2024

    GLIDEWELL HT IMPLANT Ø3.5 X 13 MM

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·May 1, 2025

    GLIDEWELL HT IMPLANT Ø3.5 X 13 MM

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT INC.·Product code DZE·April 17, 2025

    GLIDEWELL HT IMPLANT Ø3.5 X 13 MM

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC·Product code DZE·March 12, 2025

    INRATIO

    FDA Adverse Event
    Malfunction ·BIOSITE INCORPORATED·Product code JPA·March 18, 2010

    INRATIO

    FDA Adverse Event
    Malfunction ·BIOSITE INCORPORATED·Product code GJS·December 2, 2009

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·November 4, 2008

    ESSURE TUBAL LIGATION

    FDA Adverse Event
    Malfunction ·CONCEPTUS·Product code HHS·August 17, 2011

    QUADRA ASSURA CRT-D, DF4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·July 11, 2013

    LIFE SCOPE PT

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·December 26, 2023

    GLIDEWELL HT IMPLANT Ø3.5 X 13 MM

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code DZE·November 18, 2024

    LIFE SCOPE PT

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·December 8, 2023

    BioGX SARS-CoV-2 Reagents for BD MAX System-IVD PCR test intended for the qualitative detection of nucleic acid from the SARS-CoV-2 in nasopharyngeal specimens Catalog Number: 444213

    FDA Enforcement
    Class II ·Terminated·Becton Dickinson & Co.·April 21, 2021