BEUDAMED
    12 results · 18ms · Sources: EU EUDAMED, US FDA

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    BARTELS RUBEOLA IGG EIA

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111062·INSTRUMENT CASE MEDIUM ALUMINUM

    Monster Screw System

    FDA UDI
    Paragon 28, Inc.·00889795153333·K-wire, Single Ended Trocar Tip, SMOOTH, 2.3 x ...

    DEWIN

    FDA UDI
    DonneVie Medical Technology(Shanghai)Co.Ltd·16972962311375·Micromanipulation pipette is a disposable steri...

    Alleset

    FDA UDI
    GRI Medical & Electronic Technology Co., Ltd.·16931918118406·Surgical Gown_Set-In Sleeve_W/reinforcement_X-L...

    FLOWTRON FOOT GARMENT-REGULAR-STERILE FLOWTRON FOOT GARMENT-LARGE-STERILE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ALLGRAD 45 AND 90 CELL SEPARATION MEDIA

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    VERSA-DIAL/COMP TI STD TAPER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·November 4, 2020

    COMP PRIMARY STEM 11MM MINI

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·November 4, 2020

    ATTAIN OTW

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DTB·December 13, 2010

    THERMACARE MENSTRUAL HEAT

    FDA Adverse Event
    Injury ·PFIZER·Product code IMD·January 11, 2013

    WIRELESS BATTERY MODULE B

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 5, 2014