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

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    Rampart D Lumbar Interbody Fusion Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VIVID POST DRILL

    FDA UDI
    BIOLOREN SRL·08056099233302·Conical drill ø 1.2 - 1.65 mm.

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319720981·Metzenbaum Needle Holder 7-1/4" (18.4cm), stra...

    INTERLINK SYSTEM-T-CONNECTOR EXTENSION SET, MODEL 2N3326

    FDA 510(k)
    FDA Class 2 ·General Hospital

    POWDER FREE VINYL PATIENT EXAMINATION GLOVES, COLORED (YELLOW)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 13, 2011

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 10, 2013

    FLO-GARD 6301 VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FRN·September 16, 2008

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·September 11, 2022

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·April 14, 2026

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·May 24, 2021

    WEREWOLF RF 20000 CONTROLLER

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORP.·Product code GEI·June 29, 2020

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·January 11, 2022

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·January 29, 2026

    SHIRANUI HP

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·May 18, 2020

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·October 22, 2024

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 12, 2020

    SHIRANUI HP

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code LIT·April 24, 2019

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·December 6, 2024

    OHICHO3

    FDA Adverse Event
    Injury ·Product code LIT·July 19, 2019