BEUDAMED
    11 results · 26ms · Sources: EU EUDAMED, US FDA

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    DURALASTIC SHEETING II

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    P.F.C. SIGMA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295234814·P.F.C. SIGMA TC3 BOX TRIAL SZ 1.5

    NexGen®

    FDA UDI
    Zimmer, Inc.·00889024210646·

    NexGen®

    FDA UDI
    Zimmer, Inc.·00889024210653·

    NexGen®

    FDA UDI
    Zimmer, Inc.·00889024210660·

    Diagnostic Imaging Color LCD Monitor

    FDA 510(k)
    FDA Class 2 ·Radiology

    BREAS ISLEEP 20+

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PROPAQ MD DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·January 16, 2013

    EXCITE

    FDA Adverse Event
    Other ·ANSELL PROTECTIVE PRODUCTS, INC.·Product code MMS·December 1, 2010

    EON MINI

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION·Product code GZB·July 15, 2014

    Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026