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

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    CODMAN * REUSABLE PERFORATOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    EXSPIRON

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SYNTHES CRANIAL PLATES

    FDA 510(k)
    FDA Class 2 ·Dental

    MECTALIF OBLIQUE (TI PEEK) OBLIQUE INTERBODY FUSION DEVICE PEEK/TI 12XX28X9 L5°

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·December 4, 2019

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·KESTREL NO. 695 HEATER

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·KESTREL NO. 695 HEATER

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·KESTREL NO. 695 HEATER

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·KESTREL NO. 695 HEATER

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·KESTREL NO. 695 HEATER

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·KESTREL NO. 695 HEATER

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·KESTREL NO. 695 HEATER

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·KESTREL NO. 695 HEATER

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·KESTREL NO. 695 HEATER

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·KESTREL NO. 695 HEATER

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·KESTREL NO. 695 HEATER

    SMARTSETGMV ENDURANCE GENT 40G

    FDA Adverse Event
    Malfunction ·DEPUY IRELAND - 9616671·Product code LOD·July 28, 2023

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·May 14, 2014

    ENDEAVOR SPRINT RX

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code NIQ·November 6, 2012

    PROGRAMMING SOFTWARE

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·August 24, 2010

    1.85MM TI MATRIX SCREW SELF-TAPPING/4MM

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code JEY·January 21, 2015