BEUDAMED
    39 results · 19ms · Sources: EU EUDAMED, US FDA

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    MA-300 ELECTROMYOGRAPHY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    ELEVATOR

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950029792·ELEVATOR ANTRALPLASTY KIT SET OF 6 INSTRUMENTS

    ACE

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950016648·CURETTE BONE MOLT #4 6" 15CM

    6051-0000-220

    FDA UDI
    CITY TECHNOLOGY LIMITED·B404605100002200·

    CarboJet® CO2 Bone Lavage System

    FDA UDI
    Kinamed, Inc.·00898142001487·Angle Nozzle

    e-vive NMES System with Post-Op Brace; Extra Small, Left (2.0 Dock)

    FDA UDI
    Motive Health, Inc.·00854691008452·e-vive NMES System with Post-Op Brace; Extra Sm...

    Golden Isles Pedicle Screw System

    FDA UDI
    Intelivation, LLC·G079C2520002200·Curved Ti Rod, 220mm

    QB1 NMES System

    FDA UDI
    Motive Health, Inc.·00854691008292·QB1 NMES System with Post-Op Brace; XS, Left

    FOGARTY ARTERIAL CATHETER

    FDA Adverse Event
    EDWARDS CVS DIV. BAXTER HEALTHCARE CORP.·Product code DXE·December 23, 1993

    PRO-TORQ

    FDA 510(k)
    FDA Class 1 ·Dental

    MODIFICATION TO ISOBAR SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SMR GLENOID PEG TT SMALL-R #L

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·March 18, 2022

    ACCESS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - AIBONITO·Product code FPA·March 12, 2013

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC·Product code GJS·February 18, 2011

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·ANIMAS CORP.·Product code LZG·February 19, 2008

    Terumo Perfusion System 9000, 220/240v, with color screen; Model 9000; Catalog No. 164290.

    FDA Recall
    Terminated ·Terumo Cardiovascular Systems Corp·Product code DTW·September 14, 2006

    M2A 38MM MODULAR HEAD STD NECK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LZO·March 5, 2012

    TECNIS ODYSSEY TORIC II IOL

    FDA Adverse Event
    Injury ·AMO MANUFACTURING NETHERLANDS·Product code MFK·January 22, 2026

    International Technidyne Corp. (ITC) AVOXimeter 1000 Oximeter, Catalog Numbers: AVON1000-110 and AVOX-1000-220

    FDA Recall
    Terminated ·International Technidyne Corp.·Product code DQA·February 13, 2008

    TAPERLOC MODULAR FEMORAL 12.5MM X 145MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·March 5, 2012