BEUDAMED
    65 results · 22ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    EMERG. OXYGEN KIT #65350 & #65399 CASE

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    GLIDESHEATH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RADIAL HEAD IMPLANT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INTERPULSE HANDPIECE WITH COAXIAL HIGH FLOW TIP

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-PUERTO RICO·Product code FQH·May 9, 2014

    MAYFIELD 2000 SKULL CLAMP

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code HBL·October 19, 2012

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·September 18, 2007

    GLIDESHEATH

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DYB·August 7, 2019

    GLIDESHEATH

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DYB·July 7, 2022

    GLIDESHEATH

    FDA Adverse Event
    Death ·TERUMO MEDICAL CORPORATION·Product code DYB·September 6, 2023

    GLIDESHEATH

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DYB·December 1, 2020

    RADIFOCUS INTRODUCER

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DYB·May 19, 2022

    RADIFOCUS INTRODUCER

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DYB·January 21, 2022

    GLIDESHEATH

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DYB·September 28, 2023

    RADIFOCUS INTRODUCER

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DYB·June 25, 2020

    RADIFOCUS INTRODUCER

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DYB·June 25, 2020

    RADIFOCUS INTRODUCER

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DYB·June 29, 2020

    RADIFOCUS INTRODUCER

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DYB·December 2, 2021

    RADIFOCUS INTRODUCER

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DYB·May 18, 2022

    GLIDESHEATH

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DYB·October 9, 2018

    GLIDESHEATH

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DYB·November 3, 2020