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

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    ALARM INTERCOM DOOR LOCK

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Rollstand

    FDA UDI
    Bard Access Systems, Inc.·00801741124747·STANDARD ROLL STAND

    Kangaroo

    FDA UDI
    Cardinal Health 200, LLC·10192253009750·KANGAROO JOEY BLACK SUPER MINI BACKPACK

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR87700311·Mand. 2. Bicuspidband right 31

    Washbon

    FDA UDI
    ORMCO CORPORATION·00889989043600·UPPER RIGHT FIRST MOLAR WASHBON BAND SIZE 31

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR87700310101·Mand. 2. Bicuspidband right 31

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR87700310051·Mand. 2. Bicuspidband right 31

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR87700310501·Mand. 2. Bicuspidband right 31

    Internal Octa Implant System

    FDA 510(k)
    FDA Class 2 ·Dental

    MEMOMETAL MEMORY STAPLES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CAPSUREFIX NOVUS MRI SURESCAN

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·July 19, 2021

    AMPLIA MRI CRT-D SURESCAN

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code NIK·November 23, 2020

    SPRINT

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·June 27, 2019

    CAPSUREFIX NOVUS LEAD MRI SURESCAN

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·June 27, 2019

    CAPSURE SP NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·October 10, 2013

    CAPSUREFIX

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 10, 2013

    CONCERTO CRT-D DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·June 8, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·June 10, 2015

    EVERA MRI XT DR SURESCAN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LWS·June 27, 2019

    EON

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·January 28, 2014