BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    NEW HYDROPHILIC COATING FOR WIRE GUIDES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    JANUS ATAC ENG ANALYSIS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    OPTICAL VALVULOTOME

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FEMORAL STEM PRESS-FIT COLLARLESS

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·October 9, 2018

    SHELL WITH CLUSTER HOLES POROUS 58 MM O.D. SIZE LL FOR USE WITH LL LINERS

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·October 9, 2018

    LINER ELEVATED RIM 36 MM I.D. SIZE LL FOR USE WITH 58 MM O.D. SIZE LL SHELL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·October 9, 2018

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 22, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 14, 2010

    XACT CAROTID STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIM·July 9, 2014

    BIOLOX DELTA, CERAMIC FEMORAL HEAD, M, 36/0, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·October 11, 2018