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

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    Filters Regulation: Us FDA ×

    Univers Revers Modular Glenoid System (Augemented baseplates)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EarQ

    FDA UDI
    Oticon A/S·05707131342362·G10, BTE 13 2.4G 85 C093 EARQ

    NUVANT, MOBILC CARDIAC TELEMETRY

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SILS PORT MODEL SILSPT15

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    COMP RVRS 25MM BSPLT HA+ADPTR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·March 8, 2021

    KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LOX·March 17, 2020

    COBAS 6000 C501 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CEM·October 7, 2008

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·July 29, 2011

    VET LCP 2.4 12HO L96 T2 SST

    FDA Adverse Event
    Injury ·SYNTHES ELMIRA·Product code HRS·June 27, 2013

    IKAZUCHI ZERO

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LOX·June 13, 2019

    KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LOX·August 19, 2019

    IKAZUCHI ZERO

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LOX·August 20, 2019

    KANEKA PTCA CATHETER CO-R7(IKAZUCHI ZERO)

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LOX·August 21, 2019

    KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code LOX·April 14, 2022

    KANEKA PTCA CATHETER CO-R8 (TASUKI)

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LOX·December 13, 2020

    KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code LOX·December 21, 2020

    KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code LOX·April 13, 2022

    KANEKA PTCA CATHETER CO-R6 (RAIDEN3)

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LOX·June 6, 2025

    KANEKA PTCA CATHETER ZINRAI

    FDA Adverse Event
    Death ·KANEKA CORPORATION·Product code LOX·February 3, 2025

    KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LOX·December 21, 2017