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

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    ETHICON* TEMP. CARDIAC PACING WIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Bioplate®

    FDA UDI
    Bioplate, Inc.·M3848131380·Boxcar Plate - Ø1.9 mm - 4 hole - 15 x 15 mm

    Bioplate®

    FDA UDI
    Bioplate, Inc.·M384813138CP1·Boxcar Plate - Ø1.9 mm - 4 hole - 15 x 15 mm

    Bioplate®

    FDA UDI
    Bioplate, Inc.·M384813138US0·Boxcar Plate - Ø1.9 mm - 4 hole - 15 x 15 mm

    ADC COMPACT PLUS

    FDA 510(k)
    FDA Class 2 ·Radiology

    ALEUTIAN SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    JAMSHIDI BONE MARROW TRAY 11G X4 15G ASP

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code KNW·March 12, 2026

    ENDURANT II

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code MIH·May 15, 2014

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·October 31, 2012

    RESIDENT BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·August 18, 2010

    TERUMO RADIFOCUS GUIDE WIRE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 12, 2025

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 14, 2021

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·April 14, 2022

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·April 20, 2022

    RADIFOCUS GLIDEWIRE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·July 31, 2024

    RADIFOCUS GLIDEWIRE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·October 8, 2025

    JAMSHIDI BONE MARROW TRAY 11G X4 15G ASP

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code LWE·October 8, 2025

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·April 11, 2022

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·September 28, 2023

    RADIFOCUS GUIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO MEDICAL CORPORATION·Product code DQX·May 25, 2023