BEUDAMED
    14 results · 21ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    INVIGRA

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526743663·ACHIMED ACHILLES SUPP SILVER III

    Midway Select

    FDA UDI
    MIDWAY DENTAL SUPPLY, LLC·10843717102257·High Volume Evacuators, Pkg/100

    N/A

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036019488·

    EPIC SPO2 FINGER SENSOR, MODEL E412-20

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NITRILE PATIENT EXAMINATION GLOVES, POWDER-FREE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    GORE® EXCLUDER® ILIAC BRANCH ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·December 2, 2021

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·March 25, 2013

    SPEEDSCREW 5.5 MM KNOTLESS FIXATION DEVICE

    FDA Adverse Event
    Other ·ARTHROCARE CORPORATION·Product code HWC·March 9, 2011

    KION

    FDA Adverse Event
    Injury ·MAQUET CRITICAL CARE AB·Product code BSZ·March 20, 2008

    STERILE FX25RWC W/ RES

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code DTZ·April 10, 2023

    LOTUS EDGE VALVE SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NPT·November 3, 2020

    630G INSULIN PUMP MMT-1715KL 630G

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·January 19, 2023

    ENSEAL X1 CURVED 37CM SHAFT

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GEI·March 2, 2023