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

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    PEARLESCENT POWDER FREE NITRILE EXAMINATION GLOVE WITH ALOE VERA (YELLOW, RED, GREEN, BLACK, BLUE)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Bur PM2-70 80K FC Ø1.0x80 St

    FDA UDI
    Bien-Air Surgery SA·17630055519785·

    Oticon

    FDA UDI
    Oticon A/S·05707131164186·K14, RITE CBE

    AIM™FEMORAL NAIL

    FDA UDI
    Biomet Orthopedics, LLC·00887868003561·

    NITANIUM® SUPER ELASTIC ARCHWIRES

    FDA UDI
    Ortho Organizers, Inc.·00190707060152·.018 UPPER NITANIUM® SUPER ELASTIC OVAL ARCH FO...

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383501125·Gutta Percha Points is used to root canal filin...

    MOBILE-PATIENT VIEWER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AGILENT M2636A TELEMON MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AVANTAGE INLAY SIZE 50/28

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code LPH·December 15, 2016

    UNKNOWN BIOMET AVANTAGE INSERT

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LPH·February 16, 2017

    AVANTAGE E1 INSERT DIA28 S56

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·July 21, 2016

    UNKNOWN BIOMET AVANTAGE INSERT

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LPH·February 16, 2017

    G7 BISPHERICAL SHELL 50D

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·December 15, 2025

    AVANTAGE INSERT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LPH·June 2, 2017

    VASOVIEW 6 PRO

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·May 3, 2013

    GRIND NO MORE

    FDA Adverse Event
    Injury ·RANIR, LLC·Product code OBR·September 19, 2014

    ANASTOCLIP GC VESSEL CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·LEMAITRE VASCULAR, INC.·Product code FZP·May 23, 2011

    SYNCHRON SYSTEMS RHEUMATOID FACTOR REAGENT, SYNCHRON CX SYSTEMS RF CALIBRATOR

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·March 12, 2012

    SYNCHRON SYSTEMS RHEUMATOID FACTOR REAGENT, SYNCHRON CX SYSTEMS RF CALIBRATOR

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·March 12, 2012

    AVANTAGE UHMWPE INSERT

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LPH·March 29, 2017