BEUDAMED
    42 results · 34ms · Sources: EU EUDAMED, US FDA

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    WATERLASE

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

    SELEX / M2A-MAGNUM HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304477643·

    SELEX® / M2A-MAGNUM™ HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304993419·

    Audit MicroControls Control FD Assayed Chemistry, Level 1

    FDA UDI
    AALTO SCIENTIFIC·B085K0311100·

    Zavation

    FDA UDI
    Zavation LLC·00842166178540·Blades Titane

    INFINITI® Warfarin BioFilmChip® Microarray Magazine

    FDA UDI
    AUTOGENOMICS, INC·00850009370167·CYP450 2C9 drug metabolizing enzyme and VKORC1 ...

    HammerTech

    FDA UDI
    FUSION ORTHOPEDICS, LLC·00819034027125·HT PEEK Driver Medium

    QUANTA PLEX ENA PROFILE 4

    FDA 510(k)
    FDA Class 2 ·Immunology

    IDS5 IMAGE DISPLAY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    TPRLC 133 T1 PPS HO 18X156MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·February 25, 2019

    BI METRIC/XR LAT RPP C/L 8MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·June 2, 2017

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·April 2, 2013

    BRAVO PH MONITORING SYSTEM AND ACCESSORIES

    FDA Adverse Event
    Malfunction ·GIVEN IMAGING LTD.·Product code FFT·March 17, 2011

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·April 18, 2008

    UNKNOWN SELEX/MAGNUM MOD HD 40MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 21, 2013

    M/H 3HOLE RINGLOC SHELL

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LZO·March 2, 2017

    UNKNOWN E-POLY HI WALL RINGLOC ACETABULAR LINER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code MAY·February 10, 2017

    BIOMET UNKNOWN E1 MAXROM LINER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·August 8, 2018

    UNKNOWN CUP

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 8, 2018

    UNKNOWN LINER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWY·August 8, 2018