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

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    SimpliShade Bulk Fill, SimpliShade Bulk Fill Flow

    FDA 510(k)
    FDA Class 2 ·Dental

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517300188·CoRoent® XLK, 12x18x55mm 10°

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517287496·CoRoent® XL-CTW, 12x22x55mm, 10°

    Symmetry Mayo-Collins

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482147078·Symmetry® Retractor, Mayo-Collins, 6 in, (2/st)

    InCompass®

    FDA UDI
    ZIMMER SPINE, INC.·00889024400559·

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111350061·OPER SCISS DEL S/B STR 5 1/2"

    Vu aPod™ - L

    FDA UDI
    Seaspine Orthopedics Corporation·10889981046507·LATERAL TRIAL, WIDE, STANDARD, 12mm X 23mm X 55mm

    A*23 SSP UNITRAY KIT

    FDA Adverse Event
    Malfunction ·LIFE TECHNOLOGIES CORP·Product code MZI·April 7, 2014

    TSolution® One Total Knee Application

    FDA 510(k)
    FDA Class 2 ·Neurology

    Y.E.S 10 WHEELCHAIR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    HNM Medical

    FDA UDI
    HNM STAINLESS, LLC.·00842962113752·MAYO COLLINS RETRACTOR, 6", SET OF 2

    A*23 SSP UNITRAY KIT

    FDA Adverse Event
    Malfunction ·LIFE TECHNOLOGIES CORP·Product code MZI·April 7, 2014

    REVITAN, PROXIMAL PART, CONICAL, UNCEMENTED, 55, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code KWA·July 3, 2023

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·August 17, 2011

    APEX PLUS

    FDA Adverse Event
    Injury ·ALCON - ORLANDO TECHNOLOGY CENTER·Product code LZS·November 5, 2008

    ADVANTAGE SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·July 11, 2013

    CD HORIZON® SOLERA® VOYAGER¿ SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code HXX·February 4, 2026

    CD HORIZON SOLERA VOYAGER SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code HXX·February 3, 2025

    SOLERA VOYAGER 5.5

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code HXX·October 10, 2025