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

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    Filters Regulation: Us FDA ×

    Xenco Medical Cervical Interbody System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694036047·3.0/4.0mm Cannulated Headless Driver, Long

    Slap Hammer

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215046255·

    B-P TOTAL HIP SYSTEM

    FDA UDI
    ENDOTEC, INC.·00814193024084·B-P MODULAR EXTENSION W/ULTRACOAT - 13 MM X 75 MM

    TINA-QUANT HBA1C GEN.2

    FDA 510(k)
    FDA Class 2 ·Hematology

    HYDROFIX SURGICAL SHEET

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ZOLL IVTM COOL LINE CATHETER

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION·Product code NCX·June 2, 2022

    ZOLL IVTM COOL LINE CATHETER

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION·Product code NCX·February 9, 2022

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 23, 2025

    SYRINGES

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH, INC.·Product code FMF·April 20, 2016

    ATTAIN STARFIX

    FDA Adverse Event
    Malfunction ·MPRI·Product code OJX·June 10, 2013

    GOODKNIGHT 420

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code NNI·April 28, 2011

    COLLEAGUE CX VOLUMETRIC INFUSION PUMP

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

    SHIRANUI EX

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

    OHICHO3

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

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·August 14, 2020

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·September 30, 2020

    SHIRANUI EX

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·May 28, 2020

    OHICHO3

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·September 26, 2018

    OHICHO3

    FDA Adverse Event
    Injury ·Product code LIT·September 17, 2019