BEUDAMED
    13 results · 18ms · Sources: EU EUDAMED, US FDA

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    PEREGRINE SHIELDED DIFFUSION PROBE

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

    DeltaForm HD

    FDA UDI
    Merz Dental GmbH·D7091980027·DeltaForm HD lower posteriors, S, A3 -MADE IN G...

    NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·August 23, 2016

    ACCELERATOR, LINEAR, MED.

    FDA 510(k)
    FDA Class 2 ·Radiology

    ACCUSYTE 3D Fiducial Marker

    FDA 510(k)
    FDA Class 2 ·Radiology

    NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD .·Product code MCM·March 27, 2015

    NexGen®

    FDA UDI
    Zimmer, Inc.·00889024217553·

    NexGen®

    FDA UDI
    Zimmer, Inc.·00889024217560·

    ANIMAS INSULIN INFUSION PUMP

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

    UNKNOWN

    FDA Adverse Event
    Injury ·UNK·Product code FWM·January 31, 2011

    TRICUT® ANGLE-TIP BRONCHIAL BLADE

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC.·Product code EQJ·August 5, 2014

    NEXGEN ARTICULAR SURFACE

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code JWH·February 23, 2022

    Angiotech Galactography Kit. Galactography Kit 30ga with Straight Cannula and Galactography Kit 30ga with Curved Cannula. STERILE. Product Number: DGK002SX, DGK002X. 510k K980227. Qty Dist. - 2,630. MEDICAL DEVICE TECHNOLOGIES, INC. 3600 Southwest 74th Avenue, Gainesville, Florida 32608 U.S.A. Intended use: Injection Media Contrast Kit Needle

    FDA Recall
    Terminated ·Medical Device Technologies, Inc.·Product code FMI·September 1, 2009