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

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    EXMOOR SILICONE RUBBER SHEET

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

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·00636257073377·PROTECT PATELLA TRACKING BRACE, RT, LG

    Mini Master Series

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746108860·DB BKT MINI MS UR LAT 018 T+10 A+9 R=0 RAISED PAD

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756020497·FINGER SPLINTS

    Novo Surgical

    FDA UDI
    NOVO SURGICAL, INC.·G5869115030·round caps, gas or steam permeable, can be used...

    "1.5MM" SYSTEM

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036053246·

    MobileRay Pulse SE Digital Imaging System

    FDA 510(k)
    FDA Class 2 ·Radiology

    EPILATOR, BLEND-MODEL EB-200 & ET-1

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    DUROM ACETABULAR COMPONENT

    FDA Adverse Event
    Other ·ZIMMER GMBH·Product code KWA·May 27, 2014

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·January 11, 2013

    ENCORE BALLOON CATHETER INFLATION DEVICE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code MAV·December 1, 2010

    THERMOCOOL® SMART TOUCH® SF BI-DIRECTIONAL NAVIGATION CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code LPB·January 9, 2022