BEUDAMED
    30 results · 22ms · Sources: EU EUDAMED, US FDA

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    ManoScan System

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    AGC TRADITION KNEE SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304241022·

    SMITH & NEPHEW PATELLO-FEMORAL IMPLANT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    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

    TOTAL ASR ACET IMP SIZE 50

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·June 6, 2013

    HUDSON HEATED-WIRE VENTILATOR CIRCUIT W/LIMB

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BZO·June 20, 2011

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 9, 2008

    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

    PROSTHESIS, KNEE, PATELLO/FEMORAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code KRR·October 15, 2025

    PROSTHESIS, KNEE, PATELLO/FEMORAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code KRR·October 20, 2025