BEUDAMED
    31 results · 24ms · Sources: EU EUDAMED, US FDA

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    Reprocessed Harmonic Shears with Adaptive Tissue Technology (36 cm), Reprocessed Harmonic Shears with Adaptive Tissue Technology (23cm)

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

    OSS™ Orthopedic Salvage System

    FDA UDI
    Biomet Orthopedics, LLC·00880304457836·

    DM-3000 DIGITAL BLOOD PRESSURE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TAPERLOC COMPLETE

    FDA 510(k)
    FDA Class 3 ·Orthopedic

    TAPERLC BMPC LAT 6.0X132 12/14

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code KWA·August 4, 2016

    TAPERLOC PC 15.0 MM 12/14

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code KWA·August 4, 2016

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·October 10, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM VG

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·June 17, 2011

    TAPERLOC COMPLETE MICROPLASTY FEMORAL

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·January 20, 2017

    TPRLC 133 TYPE1 BM SO 11.0

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·September 12, 2018

    TAPERLOC BONEMASTER POROUS AND HYDROXYAPETITE COATED STEM

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code KWA·May 26, 2017

    TAPERLOC TYPE1 BM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·December 4, 2018

    TPRLC 133 FP TYPE1 BM HO 10.0

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·November 13, 2018

    TPRLC 133 MP TYPE1 BM HO 10.0

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 20, 2019

    TAPERLOC STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 19, 2017

    TAPERLOC FEMORAL STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·December 22, 2016

    TAPERLOC COMPLETE PRIMARY FEMORAL POROUS-BONEMASTER REDUCED DISTAL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 6, 2018

    SHORELINE ACS, WAVEFORM C

    FDA Adverse Event
    Injury ·SEASPINE ORTHOPEDICS CORPORATION·Product code OVE·November 12, 2025

    SHORELINE ACS, WAVEFORM C

    FDA Adverse Event
    Injury ·SEASPINE ORTHOPEDICS CORPORATION·Product code OVE·November 12, 2025