BEUDAMED
    15 results · 20ms · Sources: EU EUDAMED, US FDA

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    ISR'OBOT MONA LISA

    FDA 510(k)
    FDA Class 2 ·Radiology

    A.S.A.P.® Indirect+ Extraoral/HP Cylinder Adjuster Refill

    FDA UDI
    DEN-MAT HOLDINGS, LLC·00359883006136·Dental Abrasive Disk

    A.S.A.P.® Indirect+ Extraoral/HP Cylinder Adjuster Refill

    FDA UDI
    CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172016995·Dental Abrasive Disk

    LINK Instruments - Rasps, compressors and broaches

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575286324·Orthopaedic prosthesis instrument, reusable - G...

    EDWARDS LIFESCIENCES PERCUTANEOUS SHEATH INTRODUCERS WITH OLIGON MATERIAL

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CLAVICLE LOCKING PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEPUY ASR XL FEM IMP SIZE 45

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·May 24, 2013

    HOMECHOICE

    FDA Adverse Event
    BAXTER HEALTHCARE - LARGO·Product code FKX·June 16, 2011

    BLUE MAX BALLOON DILATATION CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code LIT·August 21, 2008

    OSSEOTITE TAPERED CERTAIN PREVAIL IMPLANT 4/3 X 13MM

    FDA Adverse Event
    Injury ·BIOMET 3I·Product code DZE·September 29, 2025

    H30 HOLMIUM LASER 30 WATT HOLMIUM LASER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code GEX·October 30, 2017

    H30 HOLMIUM LASER 30 WATT HOLMIUM LASER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code GEX·February 9, 2018

    H30 HOLMIUM LASER 30 WATT HOLMIUM LASER

    FDA Adverse Event
    Injury ·COOK INC·Product code GEX·February 28, 2018

    H30 HOLMIUM LASER 30 WATT HOLMIUM LASER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code GEX·February 8, 2018

    H30 HOLMIUM LASER 30 WATT HOLMIUM LASER

    FDA Adverse Event
    Injury ·COOK INC·Product code GEX·April 25, 2018