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

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    ES2 SPINAL SYSTEM MODEL 48280XXXX

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MANTIS REDUX BLOCKER

    FDA Adverse Event
    Malfunction ·STRYKER SPINE-US·Product code NKB·November 27, 2019

    ArgenZ HT+ 98x20 A2

    FDA UDI
    ARGEN CORPORATION, THE·D818122845·Dental porcelain/ceramic restoration kit

    DARCO INTERNATIONAL, INC.

    FDA registration
    DARCO INTERNATIONAL, INC.·15 products·🇺🇸 United States

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970508·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970478·

    MAHE FIXATION PLATE AND SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SAS RSV TEST

    FDA 510(k)
    FDA Class 1 ·Microbiology

    AGC DA2000 KN TIB BRG 71/75X8

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

    SM304 M-SERIES W/ZOOM

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code INK·May 21, 2013

    UNKNOWN DEPUY ASR CUP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 3, 2011

    FREESTYLE LITE

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE IN, USA·Product code LFR·August 14, 2008

    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

    UNITIP CATHETER FOR HR GI

    FDA Adverse Event
    Malfunction ·UNISENSOR USA INC·Product code FFX·January 16, 2015