BEUDAMED
    9 results · 32ms · Sources: EU EUDAMED, US FDA

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    MODEL M1251A MON. FULL DISCLOSURE REVIEW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00681490886574·INSTRUMENT 6905788 DISTRACTOR FORCEPS

    Sterngold Implant System Guided Crestal Bone Drill 5.0

    FDA UDI
    STERNGOLD DENTAL LLC·00841549118913·Used to countersink site prior to implant place...

    CLEM TM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    MODIFIED APSARA CLINICAL DIAGNOSTIC ANALYZER

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    REVERSE SHOULDER SYSTEM GLENOSPHERE 39XØ27

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·March 5, 2020

    SCREWDRIVER DUO, SW 3.5 QUICK COUPLING

    FDA Adverse Event
    Malfunction ·AAP IMPLANTATE AG·Product code HXX·May 28, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 9, 2013

    MESH - COMPOSIX KUGEL

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·November 17, 2010