BEUDAMED
    25 results · 22ms · Sources: EU EUDAMED, US FDA

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    ProLift Expandable System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517575517·CoRoent Ant TLIF Ti, 15x13x40mm 0°

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526814721·GENUMEDI PSS GREEN O

    Malibu™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981030810·PRECONTOURED ESS PLUS ROD, 5.5 x 400 mm

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100318·ALPHONSO INFANT SPECULUM

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100271·SAUER INFANT SPECULUM

    Midmark

    FDA UDI
    MIDMARK CORPORATION·00841709109539·Midmark LED retrofit kit to bring the performan...

    FLUOROMAP SOFTWARE, 9 FLUORODISC (BELT), 12 FLUORO DISC (BELT), CLOSE TUBE CLIP

    FDA 510(k)
    FDA Class 2 ·Neurology

    ACUMEN SINGLE-LUMEN DELIVERY SHEATH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ROCCIA

    FDA UDI
    Silony Medical GmbH·04054896028781·ROCCIA MultiLIF Cage 15x34 mm, 0° Lor.

    II Ring Retractor

    FDA UDI
    Automated Medical Products Corp.·00810118341540·Horizontal Solid Bar 1”

    EYE REINJECTION SET

    FDA UDI
    The Wells Johnson Company·B458201534000·Cannula Set, Eye Reinjection Set, contains: -Mi...

    COOLSCULPTING SYSTEM

    FDA Adverse Event
    Injury ·ALLERGAN PLEASANTON·Product code OOK·August 26, 2021

    RESERVOIR 3ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·October 8, 2014

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DXY·June 8, 2013

    EON MINI RECHARGEABLE IPG

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 29, 2011

    FLEXOR SHUTTLE TIBIAL GUIDING SHEATH

    FDA Adverse Event
    Injury ·COOK INC·Product code DYB·October 29, 2025

    FLEXOR SHUTTLE TIBIAL GUIDING SHEATH

    FDA Adverse Event
    Injury ·COOK INC·Product code DYB·October 29, 2025

    DYB INTRODUCER, CATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code DYB·November 12, 2025

    FLEXOR SHUTTLE SELECT GUIDING SHEATH

    FDA Adverse Event
    Injury ·COOK INC·Product code DYB·October 29, 2025