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

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    Filters Regulation: Us FDA ×

    Delta Xtend Revers Shoulder System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694015530·2.4mm x 48mm Cannulated Lag Screw

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694071000·Cannulated 2.4 x 48mm Lag Screw Sterile Qty 2

    HIVOX ELECTRIC STIMULATOR TENS & EMS, HD2

    FDA 510(k)
    FDA Class 2 ·Neurology

    PULSIOFLEX

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RHYTHMIA HDX

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQK·October 16, 2025

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Injury ·DISETRONIC MEDICAL SYSTEMS·Product code LZG·October 7, 2008

    AMS MALLEABLE 600/650 PENILE PROSTHESIS

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code FAE·July 27, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 27, 2013