BEUDAMED
    9 results · 22ms · Sources: EU EUDAMED, US FDA

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    Telemetry Monitor 5500 Release 4.0 (867232)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Integra® Miltex®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780160366·Integra® Miltex® DeBakey-Derra Anastomosis Clam...

    MODIFICATION TO CD HORIZON SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PROTOCOL Incision Dressing

    FDA 510(k)
    FDA Unclassified ·Unknown

    CD HORIZON LEGACY MINI SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS, INC.·Product code MNI·February 3, 2012

    IMMULITE 2000 XPI

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·December 12, 2019

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·November 21, 2008

    UNIFY CRT-D

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·September 11, 2011

    NATURALYTE

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·July 19, 2013