BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    SP-Fix® Spinous Process Fixation Plate, RELIEVE® Laminoplasty Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CUP: MPACT DOUBLE MOBILITY ACETABULAR SHELL Ø60

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·October 15, 2019

    Super Upper Limbs Versalock Plating System

    FDA UDI
    GM DOS REIS INDUSTRIA E COMERCIO LTDA·07901125601345·VERSALOCK CORRECTION VOLAR PLATE - 52.0x28.0mm,...

    Super Upper Limbs Versalock Plating System

    FDA UDI
    GM DOS REIS INDUSTRIA E COMERCIO LTDA·07901125601338·VERSALOCK CORRECTION VOLAR PLATE - 52.0x28.0mm,...

    COLLAGEN DENTAL MEMBRANE V

    FDA 510(k)
    FDA Class 2 ·Dental

    OSSEOSPEED TM PROFILE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    OT VERIO2 METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 18, 2016

    TOTAL CARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·June 4, 2013

    COULTER® HMX AL HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·July 27, 2011

    DUR OPT CER INS 32/54, 56

    FDA Adverse Event
    Injury ·DEPUY CORK, A DIVISION OF DEPUY ORTHOPAEDICS·Product code MRA·September 26, 2008