BEUDAMED
    30 results · 21ms · Sources: EU EUDAMED, US FDA

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    JET 1 POWERED WHEELCHAIR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Custom Procedure Kit

    FDA UDI
    MEDIVATORS INC.·40677964016583·Endo Carry-On Procedure Kit

    TECOFLEX

    FDA UDI
    Gyrus ACMI, LLC·00821925005471·7.0FR(2.3mm) X 22-28 cm QUADRA-COIL URETERAL ST...

    Sledgehammer

    FDA UDI
    Keystone Industries·H66810019701·SC 1 lb Pwd Lt Fibered Plus

    GRADIA®

    FDA UDI
    Gc America Inc.·D0470019701·GRADIA® DIRECT Unitips: 20 tips 0.16 mL A3.5

    GRADIA®

    FDA UDI
    Gc America Inc.·14548161073523·GRADIA® DIRECT Unitips: 20 tips 0.16 mL A3.5

    SCANLAN® Easy-Tag™ Tracking System

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159029253·Easy-Tag, Mini, Orange, 250/BX

    SMARTLANK WIRELESS, MODEL 001970

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    Blade Handle

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112397·BARD-PARKER HANDLE #9

    Bandtite Band Cement

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746061479·BANDTITE GLASS IONOMER CEMENT KIT

    Bandtite Band Cement

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746007842·BANDTITE GLASS IONOMER CEMENT KIT

    RADIOMED SOURCE

    FDA 510(k)
    FDA Class 2 ·Radiology

    GYRUS ENDOUROLOGY SYSTEM: AXIPOLAR RESECTOSCOPE LOOP ELECTRODE

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

    UNKNOWN MYNXGRIP

    FDA Adverse Event
    Injury ·CORDIS SANTA CLARA·Product code MGB·May 5, 2021

    ACS VIKING CORONARY GUIDING CATHETER

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code DRA·October 27, 2008

    ACS VIKING CORONARY GUIDING CATHETER

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code DRA·October 27, 2008

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·January 2, 2026

    DEXTRUS 4136

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVN·March 13, 2013

    UNICEL® DXC 600I SYNCHRON® ACCESS® CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·February 27, 2011

    TRIDENT CERAMIC INSERT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK·Product code MRA·February 21, 2008