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

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    GELITA-SPON

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    SmartArch

    FDA UDI
    ORMCO CORPORATION·00889989085792·16 DIA SMARTARCH CUNITI DAMON UPPER PK10

    IM-9A MICROINJECTORS

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    SUCTION PUMP FOR INTRACORPOREAL ULTRASOUND LITHOTRIPTER AND ACCESSORIES, MODEL 2207.XXX

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

    DELTA CER FEM HD 32/+3MM T1

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

    BIOLOX DELTA MODULAR CERAMIC HEAD 32MM STANDARD NECK TYPE 1 TAPER

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·October 18, 2016

    BIOLOX DELTA MODULAR CERAMIC HEAD 32MM STANDARD NECK TYPE 1 TAPER

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·October 18, 2016

    BIOLOX DELTA MODULAR CERAMIC HEAD 32MM STANDARD NECK TYPE 1 TAPER

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·October 18, 2016

    DELTA CERAMIC FEM HD DIA36/ 0MM 12/14

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·August 2, 2016

    ALU FEM HD D28/+3.5/5 42/12-14

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LZO·June 17, 2016

    BIOMET BONE CEMENT R 40X1

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBB·January 12, 2017

    BIOLOX DELTA INSERT 36MM 54-56MM SHELL

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·June 22, 2016

    ALU FEM HEAD D32/0/5 42/12-14

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LZO·May 16, 2016

    ALU FEM HEAD D32/-4/5 42/12-14

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LZO·May 16, 2016

    OT PING METER

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

    J-VAC RESERVOIR

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code KOG·March 14, 2011

    ONE TOUCH ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code NBW·May 23, 2008

    BIOLOX DELTA MODULAR CERAMIC HEAD

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code LZO·August 10, 2017

    G7 ACETABULAR LINER CERAMIC 32 MM F

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·January 8, 2016

    DELTA CER FEM HD 032/0MM 12/14

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·November 20, 2017