BEUDAMED
    9 results · 36ms · Sources: EU EUDAMED, US FDA

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    URODYNAMIC ANALYSIS MODULE

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

    ORTHOCON HEMASORB RESORBABLE HEMOSTATIC BONE PUTTY

    FDA 510(k)
    FDA Unclassified ·Unknown

    DISPOSABLE PNEUMOPERITONEUM NEEDLE

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

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·November 5, 2025

    G7 OSSEOTI 4 HOLE SHELL 54MM F

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·May 26, 2017

    CONSTELLATION VISION SYSTEM

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·May 21, 2014

    CONSERVE(R) PLUS SUPER FINISH FEMORAL

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code NXT·February 15, 2013

    INFINITI VISION SYSTEM

    FDA Adverse Event
    Injury ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·January 14, 2011

    Medtronic INTREPID Spinal System Coverplate, size: Small, Part Number: REF 7961330; medium, REF 7962330; large, REF 7963330; STERILE R. The INTREPID Spinal System is indicated for use with autogenous bone graft in patients with degenerative disc disease.

    FDA Recall
    Terminated ·Medtronic Sofamor Danek USA Inc·Product code MAX·February 6, 2009