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

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    VeriClear Digital Early Result Pregnancy Test

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517578044·CoRoent Ant TLIF PEEK, 8x12x32mm 8°

    PROPELLER HEAD SCREW SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304269941·

    Ada Products Company, LLC

    FDA registration
    Ada Products Company, LLC·1 product·🇺🇸 United States

    BLUNT FILL NEEDLE AND BLUNT PLASTIC CANNULA

    FDA 510(k)
    FDA Class 2 ·General Hospital

    GLUCODR PLUS SYSTEM, MODEL AGM-3000

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    MOBILELINK ACETABULAR CUP SYSTEM

    FDA Adverse Event
    Malfunction ·WALDEMAR LINK GMBH & CO. KG·Product code LPH·February 20, 2025

    CD HORIZON BALLAST SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NKB·December 9, 2019

    HEARTSTART MRX - EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 10, 2013

    V CARE STANDARD VAGINAL MANIPULATOR

    FDA Adverse Event
    Malfunction ·CONMED CORPORATION·Product code LKF·July 22, 2011

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM

    FDA Adverse Event
    Malfunction ·COSTA RICA·Product code LTI·September 29, 2008

    PEN NDL 32G 4MM PRO 100 BOX 1200 US

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMI·July 30, 2021

    BD NANO¿ 2ND GEN PEN NEEDLES 32G X 4MM (100 COUNT)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·October 25, 2023

    BD PEN NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·February 23, 2021