BEUDAMED
    18 results · 22ms · Sources: EU EUDAMED, US FDA

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    Navigated Anterolateral Disc Prep Instruments

    FDA 510(k)
    FDA Class 2 ·Neurology

    RADIAL JAW 4 PULMONARY STANDARD CAPACITY BIOPSY FORCEPS; RADIAL JAW 4 PULMONARY STANDARD CAPACITY BIOPSY FORCEPS WITH NE

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    C-THRU SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NEOCIF INSERTION INSTRUMENT

    FDA Adverse Event
    Malfunction ·BIOMET SPAIN, S.L.·Product code MQP·November 6, 2018

    ACCESS® 2 IMMUNOASSAY SYSTEM, SINGLE SYSTEM SG

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·October 21, 2011

    ACCESS® 2 IMMUNOASSAY SYSTEM, SINGLE SYSTEM SG

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·October 21, 2011

    ACCESS® 2 IMMUNOASSAY SYSTEM, SINGLE SYSTEM SG

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·October 21, 2011

    NEOCIF INSERTION INSTRUMENT

    FDA Adverse Event
    Malfunction ·BIOMET SPAIN, S.L.·Product code MQP·July 20, 2017

    TPRLOC COCR CMTD STM T1 12.5MM

    FDA Adverse Event
    Death ·BIOMET UK LTD.·Product code JDI·March 23, 2026

    ACCESS® 2 IMMUNOASSAY SYSTEM, SINGLE SYSTEM SG

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·October 28, 2011

    CMK MOD 12/14 SZ202 L130

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LZO·November 24, 2025

    QUICKFLEX MICRO LV LEAD

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISI·Product code NIK·January 11, 2014

    2.7MM TI CORTEX SCREW SLF-TPNGWITH T8 STARDRIVE RECESS 34MM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·June 27, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·August 4, 2011

    UNICEL® DXI 600 ACCESS IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code LOM·March 29, 2012

    UNICEL DXI 800 ACCESS® IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·September 2, 2011

    REVITAN, DISTAL PART, CURVED, UNCEMENTED, 24/200

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code KWY·July 20, 2023

    CMK MOD 12/14 SZ202 L130

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·January 8, 2026