BEUDAMED
    25 results · 23ms · Sources: EU EUDAMED, US FDA

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    PLEURX PERITONEAL CATHETER KIT AND PLEURX DRAINAGE KITS

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

    Acu-Tip Electrosurgical Cauterizing Instrument

    FDA UDI
    PRACTICON, INC.·00723896003244·Electrosurgical instrument

    M2410B IMAGEPOINT HX MULTISPECIALTY SYSTEM, VERSION B.1

    FDA 510(k)
    FDA Class 2 ·Radiology

    MODIFICATION TO EBI EFIX VISION FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    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

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·April 10, 2013

    ACCU-CHEK AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS CORP.·Product code LFR·May 19, 2008

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·April 12, 2011

    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