BEUDAMED
    27 results · 23ms · Sources: EU EUDAMED, US FDA

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    MODIFIED CRP LATEX TEST

    FDA 510(k)
    FDA Class 2 ·Immunology

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00885074246383·INSTRUMENT 8880016 SILO 5.5M SDE HK PSHR

    Trimline

    FDA UDI
    ORMCO CORPORATION·00889989052206·LOWER RIGHT SECOND MOLAR TRIMLINE BAND SIZE 16

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867385528·Drill Bit, 1.7mm, Long

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209132782·

    Dna-Probe, B And T Lymphocyte

    FDA Pre-Market Approval
    FDA Class 2 ·ONCOR B/T GENE REARRANGEMENT TEST

    Home Use IPL Beauty Device

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    NRBC-CHEX FOR ADVIA

    FDA 510(k)
    FDA Class 2 ·Hematology

    NexGen®

    FDA UDI
    Zimmer, Inc.·00889024199170·

    NexGen®

    FDA UDI
    Zimmer, Inc.·00889024199163·

    Dna-Probe, B And T Lymphocyte

    FDA Pre-Market Approval
    FDA Class 2 ·ONCOR B/T GENE REARRANGEMENT TEST

    Dna-Probe, B And T Lymphocyte

    FDA Pre-Market Approval
    FDA Class 2 ·ONCOR B/T GENE REARRANGEMENT TEST

    Dna-Probe, B And T Lymphocyte

    FDA Pre-Market Approval
    FDA Class 2 ·ONCOR B/T GENE REARRANGEMENT TEST

    Dna-Probe, B And T Lymphocyte

    FDA Pre-Market Approval
    FDA Class 2 ·ONCOR B/T GENE REARRANGEMENT TEST

    NEXGEN COMPLETE KNEE SOLUTION ROTATING HINGE KNEE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code KRO·November 1, 2016

    UNKNOWN_RECONSTRUCTIVE_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code KWA·June 18, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 13, 2010

    PROPLEGE CORONARY SINUS CATHETER

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code DWF·December 19, 2012

    NEXGEN ROTATING HINGE KNEE ARTICULAR SURFACE WITH HINGE POST EXTENSION

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code KRO·August 26, 2016

    NEXGEN COMPLETE KNEE SOLUTION ROTATING HINGE KNEE TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KRO·December 10, 2018