BEUDAMED
    30 results · 26ms · Sources: EU EUDAMED, US FDA

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    Cortical Fixation Systems

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AVANOS

    FDA UDI
    Avanos Medical, Inc.·00193493929207·AVANOS* Universal Block Trays

    Halyard

    FDA UDI
    Avanos Medical, Inc.·10680651929201·HYH,UBLOCK,UBT,-,-,10

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515024977·Boley Retractor, D/E 1/2" x 7/16", 6 1/4" L

    TAPERLOC COMPLETE

    FDA 510(k)
    FDA Class 3 ·Orthopedic

    PORTEX BLUE LINE SACETT SUCTION ABOVE THE CUFF TRACHEAL TUBE, SIZE 6.0 AND 6.5, 7.0 AND 7.5, 8.0 AND 8.5, 9.0

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    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

    PK DISSECTING FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·June 20, 2013

    SEPRAFILM (SODIUM HYALURONATE, CARBOXYMETHYLCELLULOSE) MEMBRANE

    FDA Adverse Event
    Injury ·GENZYME BIOSURGERY (SEPRAFILM/PACK)·Product code MCN·July 22, 2011

    PRIMARY PLUM SET WITH CONV PINK, SEC CAP PORT, 1 CL

    FDA Adverse Event
    Malfunction ·HOSPIRA DE COSTA RICA LTD.·Product code FPA·September 29, 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

    DR FOG TREATED SPONGE, STERILE

    FDA Adverse Event
    Malfunction ·ASPEN SURGICAL PRODUCTS, CALEDONIA·Product code OCT·September 16, 2020