BEUDAMED
    35 results · 28ms · Sources: EU EUDAMED, US FDA

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    Elos Accurate Hybrid Base

    FDA 510(k)
    FDA Class 2 ·Dental

    DJO SURGICAL

    FDA UDI
    Encore Medical, L.P.·00190446922780·SPECIAL, EMPOWR CAPPED OFFSET ACET. IMPACTOR

    NuVasive

    FDA UDI
    Nuvasive, Inc.·00195377046420·NTS Standard Tube, 18x60mm

    Ion Coagulation Pen

    FDA UDI
    ION MEDICAL, INC.·B9122018602·18 Gauge Curved Bipolar Coagulation Pen

    CODMAN

    FDA UDI
    Cerenovus, Inc.·10886704002451·CODMAN Slimline Temporary Aneurysm Clip No 6 Bl...

    5 ML BD¿ PRE-FILLED NORMAL SALINE SYRINGE, IN 10 ML SYRINGE

    FDA Adverse Event
    Injury ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FOZ·May 1, 2018

    BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code QJR·July 17, 2020

    NOVABONE PUTTY- BIOACTIVE SYNTHETIC BONE GRAFT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PARASPA PARAFFIN BATH, PARASPAP MINI, PARASPA ULTRA

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Widex

    FDA UDI
    Widex A/S·05706069728262·Widex EVOKE E-FS (Silver Grey S-330 ) Telecoil,...

    UNKNOWN LIGASURE INSTRUMENT

    FDA Adverse Event
    Injury ·COVIDIEN MFG DC BOULDER·Product code GEI·March 21, 2019

    SPIDER FX

    FDA Adverse Event
    Injury ·COVIDIEN·Product code NTE·November 8, 2018

    PUMP MMT-512LNAB PRDGM INS BL EN US LN

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code LZG·October 15, 2008

    SPRINT QUATTRO SECURE S

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·August 11, 2011

    TREATMENT RECLINER

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FRK·July 2, 2013

    SPIDER FX

    FDA Adverse Event
    Injury ·COVIDIEN·Product code NTE·November 8, 2018

    PROTEGE RX CAROTID STENT SYSTEM

    FDA Adverse Event
    Injury ·COVIDIEN·Product code NIM·March 23, 2018

    HEARTMATE 3 LVAS IMPLANT KIT

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·September 17, 2023

    GREENLIGHT MOXY FIBER OPTIC

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INC.·Product code GEX·October 18, 2018

    AMPLATZER OCCLUDER (UNKNOWN)

    FDA Adverse Event
    Injury ·AGA MEDICAL CORPORATION·Product code MLV·July 20, 2020