BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    ETEST FOR CEFUROXIME

    FDA 510(k)
    FDA Class 2 ·Microbiology

    CAPSTONE® Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994387295·SPACER 2990722 CAPSTONE PEEK 07X22

    CAPSTONE SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·January 13, 2016

    TriMAX Implant System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SHAPE-HF CARDIOPULMONARY EXERCISE TESTING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·August 21, 2014

    PUMP 381 PUMP SET (US)

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code OZD·January 15, 2026

    AC-POWERED ADJUSTABLE HOSPITAL BED, INCLUDING RAILS

    FDA Adverse Event
    Malfunction ·CARROLL HEALTHCARE·Product code FNL·March 5, 2013

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·February 8, 2011

    SPRINT QUATTRO SECURE S

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·August 8, 2014