BEUDAMED
    14 results · 21ms · Sources: EU EUDAMED, US FDA

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    Prase MIS Spinal System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Bernafon

    FDA UDI
    Bernafon AG·05711584077269·AQ CO7 B 105, 2.4G NFM DPB SABE/MSIL ACCUQ

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515026292·Deaver Ret, hollow hndl, 50mm, 12 1/2"

    PITUITARY RONGEUR-STRAIGHT 4MM WIDTH

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTD·May 11, 2021

    LAG SCREW, TI GAMMA3 10.5X95MM

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·October 25, 2012

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970010·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970027·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172974018·UniTip High Resolution Catheter 10F

    AUTOCLAVABLE CAMER HEAD MODEL OTV-Y0017

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

    ANGIOSCULPT PTA SCORING BALLOON CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GMK-HINGE FIXED TIBIAL INSERT SIZE 5/20MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·December 28, 2022

    COLLEAGUE CX VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 2, 2008

    XENFORM

    FDA Adverse Event
    Other ·TEI BIOSCIENCES INC·Product code FTM·June 17, 2013

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD·Product code MCM·July 28, 2011