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

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    Filters Regulation: Us FDA ×

    Nitrile Glove Powder Free Black

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PROPELLER HEAD SCREW SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304270305·

    SNOR-SCOPE PLUS OR SNOR-SCOPE + ELECTRONIC STETHOSCOPE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    N-FORCE FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    STEM: AMISTEM P STD STEM SIZE 4

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·December 30, 2020

    HARMONIC ACE 36 CM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code LFL·October 3, 2008

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·June 21, 2013

    HUDSON CONCHATHERM NEPTUNE HEATED HUMIDIFIER

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BTT·July 8, 2011