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

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    Filters Regulation: Us FDA ×

    Ni2 Implant System

    FDA 510(k)
    FDA Class 2 ·Dental

    BD BBL™ Mycosel™ Agar Deep Fill

    FDA UDI
    BECTON, DICKINSON AND COMPANY·10382902218477·Plate Mycosel Agar Deep Fill 20 Ea

    PEDICLE SCREW MUST COMBINED SETSCREW H4-T27 - (4X)

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKB·October 13, 2022

    TITAN

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    BIOPSY SCIENCES, LLC. MAXI-CELL BIOPSY NEEDLES

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

    LUMAX 340 VR-T

    FDA Adverse Event
    Injury ·BIOTRONIK GMBH AND CO.·Product code LWS·November 3, 2008

    POWER PRO AMBULANCE COT

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code INK·July 21, 2011

    AP STD, ACCESS PORT KIT RAPIDPORT EZ

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·July 9, 2013

    BD NEXIVA CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Injury ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·July 10, 2020

    BD NEXIVA CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Injury ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·July 10, 2020