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

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    TR90BH

    FDA 510(k)
    FDA Class 2 ·Radiology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814701·GENUMEDI SILVER SIZE VII

    AVANOS

    FDA UDI
    Avanos Medical, Inc.·00193493934010·AVANOS* Single-Shot Epidural Trays

    Halyard

    FDA UDI
    Avanos Medical, Inc.·10680651934014·HYH,EP TRY,S-SHOT,-,-,10

    Ophthalmic Retractor

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100974·DESMARRES LID RETRACTOR #2

    MEDTRONIC NEUROMODULATION

    FDA registration
    MEDTRONIC NEUROMODULATION·26 products·🇺🇸 United States

    ORTHOCAD IQ

    FDA 510(k)
    FDA Class 2 ·Dental

    FIBER FORCE

    FDA 510(k)
    FDA Class 2 ·Dental

    UNKNOWN_PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·April 25, 2014

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·December 1, 2008

    ENTERRA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LNQ·August 5, 2014

    2182207-2009-07584

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·March 11, 2009

    2182207-2009-07623

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·March 11, 2009

    2182207-2021-02220

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·December 22, 2021

    2182207-1997-00122

    FDA Adverse Event
    Injury ·MEDTRONIC INC.·Product code LKK·April 11, 1997

    2182207-1997-00059

    FDA Adverse Event
    Malfunction ·Product code GZB·June 13, 1997

    2182207-1997-00023

    FDA Adverse Event
    Other ·MEDTRONIC INC.·Product code GZB·April 8, 1997

    2182207-2020-01123

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·October 22, 2020

    2182207-2021-01645

    FDA Adverse Event
    Malfunction ·Product code LKK·September 23, 2021

    2182207-2000-00068

    FDA Adverse Event
    Malfunction ·Product code GZB·February 24, 2000