BEUDAMED
    27 results · 25ms · Sources: EU EUDAMED, US FDA

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    RETROGRADE CARDIOPLEGIA CANNULA, SELF-INFLATING, WITH MALLEABLE OR GUIDEWIRE STYLET

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040128671·Elevator Cryer #34

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092002019·artVeneer life lower posteriors, XS, A2

    GEN4 DIGITAL

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828177436·GEN4 DIGITAL

    Battalion

    FDA UDI
    ALPHATEC SPINE, INC.·00840967188614·Battalion, LLIF Trial, 0°, 20 mm Wide, 19 mm X ...

    DULBECCO'S MODIFIED EAGLE'S MEDIUM NO. 200-2019

    FDA 510(k)
    FDA Class 1 ·Hematology

    Pure EP - 5 x 10 pin Yoked Jumper Cable White

    FDA UDI
    BIOSIG TECHNOLOGIES, INC.·00856750007130·5 cables in one bag with 10 pin yoked jumper ca...

    TI500 GLOBE-TROTTER TRANSPORT SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SINGLE SIZE TENDON SPACER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523127221·Straight Acetabular 6.5mm Tap Guide

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523122028·19mm Bullet Nose Distractor

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523120086·Angled Drill Guide

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·January 3, 2025

    CEMENT, BONE, VERTEBROPLASTY

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NDN·April 29, 2019

    CEMENT, BONE, VERTEBROPLASTY

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NDN·April 29, 2019

    UNKNOWN PARIETEX PRODUCT

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION SAS·Product code FTL·May 13, 2019

    ZNN CMN LAG SCREW 10.5X105

    FDA Adverse Event
    Other ·ZIMMER GMBH·Product code HSB·March 11, 2013

    HOMECARE HUMIDIFIER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTT·February 27, 2011

    EEA 31MM SINGLE-USE STAPLER

    FDA Adverse Event
    Injury ·NORTH HAVEN - USS·Product code GAG·February 22, 2008

    12/14 ARTICUL 40MM M SPEC+12

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·February 13, 2019