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

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    TinniLogic Mobile Tinnitus Management Device

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

    ORTHODONTIC CERAMIC BRACKETS

    FDA 510(k)
    FDA Class 2 ·Dental

    VIGILEO ARTERIAL PRESSURE CARDIAC OUTPUT / OXIMETRY MONITOR; VIGILEO APCO / OXIMETRY MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GM HELIX ACQUA IMPLANT,TI,5.0X16

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·May 16, 2018

    GM HELIX IMPLANT 4.3X13

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·June 6, 2018

    GM HELIX IMPLANT 4.3X13

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·June 22, 2018

    GM DRIVE ACQUA IMPLANT 3.5X8 MM

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·August 29, 2018

    GM HELIX ACQUA IMPLANT 3.75X11.5

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·April 24, 2018

    AMISTEM H, HA COATED STEM SIZE 3 STD

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·February 22, 2017

    GM HELIX IMPLANT 3.5X10

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·June 29, 2018

    GM HELIX ACQUA IMPLANT 3.5X11.5

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·April 24, 2018

    GM DRIVE IMPLANT 3.5X10

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·April 20, 2018

    SURGICAL STAINLESS STEEL SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC·Product code GAQ·July 15, 2011

    RESTORE ULTRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·June 11, 2013

    SENSORMEDICS

    FDA Adverse Event
    Injury ·CARDINAL HEALTH 207, INC.·Product code LSZ·September 16, 2008

    RADIFOCUS GLIDEWIRE ADVANTAGE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 1, 2020

    GLIDEWIRE ADVANTAGE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·July 9, 2025

    RADIFOCUS GLIDEWIRE ADVANTAGE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 23, 2022

    RADIFOCUS GLIDEWIRE ADVANTAGE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·February 3, 2025

    RADIFOCUS GUIDEWIRE ADVANTAGE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·July 12, 2024