BEUDAMED
    58 results · 22ms · Sources: EU EUDAMED, US FDA

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    ORBIT

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ArgenPMMA 98x20-B4

    FDA UDI
    ARGEN CORPORATION, THE·D818120880·Crown And Bridge, Temporary, Resin

    GentleLASE

    FDA UDI
    Candela Corporation·00817495020693·Pulsed Laser

    MARKNEW PRODUCTS ACUPUNCTURE NEEDLES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BRIGHTWAY TM BRAND NITRILE EXAMINATION GLOVES, POWDER FREE, NON-STERILE. (GREY COLOR)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    36MM COCR MOD HD STD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·May 26, 2021

    ACETABULAR APEX PLUG

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·May 26, 2021

    TI LOW PROFILE SCREW 6.5X35MM IA6.5X35MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·May 26, 2021

    M/H 3HOLE RLC SHL NRS 56MM/L24

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·May 26, 2021

    ARCOMXL 36MM RLC LNR MROM SZ24

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·May 26, 2021

    TPRLC 133 T1 PPS HO 11X142MM 2MM T1

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·May 26, 2021

    EDWARDS SAPIEN TRANSCATHETER HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·May 20, 2013

    INTERSTIM

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·September 26, 2014

    CARPENTIER-EDWARDS BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·June 11, 2011

    SYRINGE 20ML LS PRECISE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FMF·July 15, 2020

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORP.·Product code OKS·August 19, 2014

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·January 13, 2017

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016