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

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    EMBRYO TRANSFER CATHETER SET, MODEL 320200 AND 320201

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·10304040094355·Maxima Hedstrom Files 25mm

    NA

    FDA UDI
    Richard Wolf GmbH·04055207063453·ESWL TREATMENT TABLE Multifunctional treatment...

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092117163·Nobel Active/Conical RP Titanium Screw

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·H65810009501·FILES HEDSTROM #45 25MM

    Implant Prosthetics

    FDA UDI
    Preat Corporation·10842092117160·Nobel Active/Conical RP Titanium Screw (10-Pack)

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361008255·PedFuse ReTurn, Hex, CNL, 9.0mm x 50mm

    SILHOUETTE PARADIGM

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·October 30, 2024

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·July 29, 2024

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·May 22, 2024

    TOP QUALITY CHLORINATED-POWDERFREE EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CAUTERY FORCEPS WITH FOOTSWITCH

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code NIQ·June 19, 2009

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·November 11, 2024

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·November 20, 2024

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·January 26, 2025

    Clarius Ultrasound Scanner

    FDA UDI
    Clarius Mobile Health Corp·07540205000595·Clarius brand C3 Premium scanner

    Clarius Ultrasound Scanner

    FDA UDI
    Clarius Mobile Health Corp·07540205000199·ARTHREX Synergy Curvilinear Scanner

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 13, 2013

    SJM EPIC STENTED TISSUE VALVE

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL BRASIL LTDA.·Product code LWR·February 18, 2011