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

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    Stryker Facial iD Plating System

    FDA 510(k)
    FDA Class 2 ·Dental

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517638953·CoRoent Ant TLIF PEEK, 8x12x30mm 15°

    AED

    FDA UDI
    NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.·00848657016179·Hysteroscopy Examination Sheath, 4mm, 30*

    Ophthalmic Retractor

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100981·DESMARRES LID RETRACTOR #3

    HASS ZIRTOOTH MODEL ZORTOOTH H. ZIRTOOTH T. ZIRTOOTHC, ZIRTOOTH P

    FDA 510(k)
    FDA Class 2 ·Dental

    G2 EXPRESS FILTER SYSTEM - FEMORAL AND JUGULAR/SUBCLAVIAN DELIVERY KITS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HOYER 600

    FDA Adverse Event
    Malfunction ·BHM MEDICAL, INC.·Product code FNG·May 13, 2011

    2182305-1999-00032

    FDA Adverse Event
    Other ·December 22, 1999

    2182305-1999-00031

    FDA Adverse Event
    Other ·December 22, 1999

    2182305-1999-00033

    FDA Adverse Event
    Other ·December 22, 1999

    HOYER 600

    FDA Adverse Event
    Malfunction ·ARJOHUNTLEIGH MAGOG INC·Product code FSA·January 22, 2013

    MEDFUSION

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·February 6, 2023

    HOYER 600

    FDA Adverse Event
    Malfunction ·ARJOHUNTLEIGH MAGOG·Product code FSA·February 17, 2012

    HOYER LIFT

    FDA Adverse Event
    APEX HEALTHCARE MFG INC·Product code FNG·June 15, 2006

    HOYER LIFT

    FDA Adverse Event
    Other ·APEX HEALTHCARE MFG. INC·Product code FSA·June 26, 2006

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·June 10, 2013

    INTERSTIM

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code EZW·July 11, 2011

    HIRES 90K

    FDA Adverse Event
    Malfunction ·ADVANCED BIONICS LLC·Product code MCM·September 30, 2008

    MENTOR CPX4 WITH SUTURE TABS, TALL HEIGHT, SMOOTH

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code LCJ·October 24, 2019

    MENTOR CPX4 WITH SUTURE TABS, MED HEIGHT, SMOOTH

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code LCJ·January 10, 2020