BEUDAMED
    10 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    PureLift

    FDA 510(k)
    FDA Class 2 ·Neurology

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306804472·Robotti Micro Elevator, 3mm, 16cm

    SURESTEP

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·September 18, 2002

    NOVATION CROWN CUP GXL LINERS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AIRSTRIP OB

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

    DELTRAN PLUS

    FDA Adverse Event
    Malfunction ·UTAH MEDICAL PRODUCTS, INC.·Product code CBT·February 12, 2020

    ESSURE

    FDA Adverse Event
    Injury ·Product code HHS·October 14, 2014

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·July 19, 2011

    6000CMS

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·June 10, 2013

    INSTINCT PLUS ENDOSCOPIC CLIPPING DEVICE

    FDA Adverse Event
    Malfunction ·COOK ENDOSCOPY·Product code PKL·September 16, 2021