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

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    LIQUID ENZYME ID 90133

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981561·anteriors; shade A2 light; mould UL2

    ANGIOGRAPHIC GUIDE WIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OSFERION D

    FDA 510(k)
    FDA Class 2 ·Dental

    CER BIOLOXD MOD HD 36MM -3 NK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·March 14, 2018

    G7 NEUTRAL E1 LINER 36MM F

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PBI·March 14, 2018

    TAPERLOC 133 TYPE1 PPS SO 13.0

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 14, 2018

    ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWQ·February 27, 2013

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·January 31, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 5, 2014

    CER BIOLOXD MOD HD 36MM -3 NK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·March 14, 2018

    G7 NEUTRAL E1 LINER 36MM F

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PBI·March 14, 2018

    TPRLC 133 TYPE1 PPS SO 13.0

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 14, 2018