BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    WIELISA ANCA SCREENING KIT TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Immunology

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981748·anteriors; shade D3 light; mould UM8

    Magnesium

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    ONEPLANT DENTAL IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    G7 NEU +5MM E1 LINER 40MM F

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·November 12, 2021

    ASR ACETABULAR CUPS 54

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·February 27, 2013

    COLLEAGUE CX TRIPLE CHANNEL VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·February 8, 2011

    UNKNOWN HIP

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·August 5, 2014

    ALINITY C MAGNESIUM

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code JGJ·February 16, 2026

    Clinical Chemistry Albumin BCG (AlbG) List Number 7D53-21 Clinical Chemistry Albumin BCG 510(k) K981758, Product Code CIX The Albumin BCG assay is used for the quantitation of albumin in human serum or plasma

    FDA Recall
    Terminated ·Abbott Laboratories Inc.·Product code CIX·March 10, 2010