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

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    TITANIUM CANNULATED INTERFERENCE SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NVM5

    FDA UDI
    Nuvasive, Inc.·00887517141095·NVM5 PM, 2+SSEPs

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707066231·PREFORMED LIGATURE WIRE 012"

    2040 Ceramic Brackets

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746005367·COSMETIC 20/40 LOWER ANT 022 T=0 A=0 R=0

    ULTRAPOWER

    FDA UDI
    Conmed Corporation·10845854002520·ULTRAPOWER BUR, ROUND(RED), 6.5 MM

    RESPIRATORY BELT SENSOR, MODEL 6000S; LIMB MOVEMENT SENSOR, MODEL 3000S

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    AESCULAP -MIETHKE SHUNT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    VITAL SIGNS® EXTRA LARGE FACE MASK WITH ADJUSTABLE AIR CUSHION SIZE 6X

    FDA Adverse Event
    Malfunction ·Product code CAI·June 28, 2021

    ARTICULEZE M HEAD 36MM +12

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code JDI·March 26, 2013

    SPRINT FIDELIS

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·March 16, 2011

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·March 26, 2008

    HEARTMATE II LVAS IMPLANT KIT (WITH SEALED GRAFTS)

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·June 15, 2021

    ID NOW COVID 19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·October 5, 2021

    ID NOW COVID 19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·October 5, 2021

    ID NOW COVID 19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·October 5, 2021

    SORIN BIOMEDICA SMARXT BCD VANGUARD

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTR·November 20, 2019

    UNKNOWN FEMORAL COMPONETN

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 24, 2023

    BIOMET FINNED PRI STEM 40MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 24, 2023

    SORIN BIOMEDICA SMARXT BCD VANGUARD SURFACE MODIFIED BLOOD CARDIOPLEGIA SYSTEM

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTR·November 16, 2016

    MUSC CHARLESTON SC 1

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DWF·March 28, 2012