BEUDAMED
    48 results · 21ms · Sources: EU EUDAMED, US FDA

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    System, Nuclear Magnetic Resonance Imaging

    FDA Pre-Market Approval
    FDA Class 2 ·INSTRUMENTARIUM ULF MR IMAGING SYSTEM

    System, Nuclear Magnetic Resonance Imaging

    FDA Pre-Market Approval
    FDA Class 2 ·ACUTSCAN MODEL 100 MRI SYSTEM

    System, Nuclear Magnetic Resonance Imaging

    FDA Pre-Market Approval
    FDA Class 2 ·INSTRUMENTARIUM ULF MR IMAGING SYSTEM

    PREMIER® Anterior Cervical Plate System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00681490482011·SCREW 6860010 VAST CNCLLS 4.0X10MM

    Trimline

    FDA UDI
    ORMCO CORPORATION·00889989051513·UPPER RIGHT SECOND MOLAR TRIMLINE BAND SIZE 10

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613153161875·PLATE BENDING PLIERS FOR CS PLATES

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613327300116·PEEK CUSTOMIZED COMPLEX-PLUS-S

    NTI

    FDA UDI
    NTI - Kahla GmbH Rotary Dental Instruments·E310860010CFG1·NTI Diamond Coarse FG

    Plateau-X Spacer System

    FDA UDI
    Life Spine, Inc.·00190837015985·

    UNITRAY A LOCUS SSP

    FDA Adverse Event
    Malfunction ·Product code MZI·September 26, 2013

    Separator, Automated, Blood Cell And Plasma, Therapeutic

    FDA Pre-Market Approval
    FDA Unclassified ·CURESIS PLASMA SEPARATOR

    Stent, Urethral, Prostatic, Semi-Permanent

    FDA Pre-Market Approval
    FDA Class 3 ·THE SPANNER TEMPORARY PROSTATIC STENT

    APEX MONORAIL

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code LOX·June 19, 2009

    APEX MONORAIL

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code LOX·June 8, 2009

    AS COLUMBUS CR FEMORAL COMP.CEMENTED F4R

    FDA Adverse Event
    Death ·AESCULAP AG·Product code JWH·October 5, 2022

    A LOCUS SSP UNITRAY KIT

    FDA Adverse Event
    Malfunction ·LIFE TECHNOLOGIES CORPORATION·Product code MZI·December 26, 2013

    MAVERICK2 MONORAIL PTCA CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code LOX·April 19, 2007

    Stent, Urethral, Prostatic, Semi-Permanent

    FDA Pre-Market Approval
    FDA Class 3 ·THE SPANNER TEMPORARY PROSTATIC STENT AND ACCESSORIES

    Stent, Urethral, Prostatic, Semi-Permanent

    FDA Pre-Market Approval
    FDA Class 3 ·SPANNER TEMPORARY PROSTATIC STENT WITH DISTAL CURVE DESIGN CHANGE

    Stent, Urethral, Prostatic, Semi-Permanent

    FDA Pre-Market Approval
    FDA Class 3 ·THE SPANNER TEMPORARY PROSTATIC STENT