BEUDAMED
    51 results · 28ms · Sources: EU EUDAMED, US FDA

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    FISIO CHAMBER SPACE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Ultra-Pro e™ Variable Angle Needle Guide

    FDA UDI
    CIVCO MEDICAL INSTRUMENTS CO., INC.·10841436102220·Sterile needle guide

    Clean-Bor Tube 1-3/8" x 36"

    FDA UDI
    Vacumed·00850644007749·Clean-Bor Tube

    OrthoMedFlex

    FDA UDI
    ORTHOMEDFLEX LLC·M7161011360·Slap Hammer

    AIM™FEMORAL NAIL

    FDA UDI
    Biomet Orthopedics, LLC·00887868003318·

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450189597·

    Mercodia C-peptide ELISA

    FDA UDI
    Mercodia AB·07350108630085·Mercodia C-peptide ELISA provides a method for ...

    CORDIS INTRODUCER GUIDE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    APEX FIXATION PINS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Widex

    FDA UDI
    Widex A/S·05706069710144·Widex EVOKE E-PA (Deep Blue ) RC coil

    Widex

    FDA UDI
    Widex A/S·05706069885620·WIDEX MOMENT MRB0 (Deep Blue ) RIC 10

    AVANTAGE INLAY SIZE 50/28

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code LPH·December 15, 2016

    UNKNOWN BIOMET AVANTAGE INSERT

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LPH·February 16, 2017

    AVANTAGE E1 INSERT DIA28 S56

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·July 21, 2016

    UNKNOWN BIOMET AVANTAGE INSERT

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LPH·February 16, 2017

    PRECISION NOVI

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·November 29, 2022

    G7 BISPHERICAL SHELL 50D

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·December 15, 2025

    AVANTAGE INSERT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·June 2, 2017

    FORTIFY ASSURA DR, DF4 CONNECTOR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 9, 2013

    GREENLIGHT HPS BPH FIBER OPTIC

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·September 19, 2014