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

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    Filters Regulation: Us FDA ×

    NUVASIVE BENDINI SPINAL ROD BENDING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    No Brand

    FDA UDI
    Smith & Nephew, Inc.·03596010069658·STAINLESS STEEL HALF PIN 4MM X 30MM

    ArgenZ HT+ 95x18 C1

    FDA UDI
    ARGEN CORPORATION, THE·D818122742·Dental porcelain/ceramic restoration kit

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·May 8, 2013

    AUDIT MICROLQ SPINAL FLUID CONTROL

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    NASAL CEASE

    FDA 510(k)
    FDA Unclassified ·Unknown

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·January 30, 2015

    AGC DA2000 KN TIB BRG 71/75X8

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·April 9, 2026

    PROXIMATE ILS CURVED CIR STAPL

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·May 21, 2013

    PINNACLE 300 ACET CUP 50MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·June 3, 2011

    UNK DEPUY ACS LINER

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWB·August 15, 2008

    VAPR3 GENERATOR *EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code GEI·December 26, 2018

    VANGUARD ROCC POR FEM S55 R

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code MBH·January 22, 2026

    VANGUARD ROCC POR FEM S57.5 L

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code MBH·January 22, 2026

    VANGUARD ROCC POR FEM S57.5 L

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBH·May 13, 2025

    TINBN VANGUARD INT PS ANAT FM R 75MM

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code MBH·June 4, 2025

    VANGUARD ROCC POR FEM S55 R

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code MBH·June 4, 2025