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

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    BIOTEQUE VAGINAL DILATOR

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

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092103005·CAMLOG® Screw-Line-compatible 3.8mm 17° Multi-U...

    t:slim Cartridge 10 Pack

    FDA UDI
    Tandem Diabetes Care, Inc.·00852162004347·t:slim Cartridge 10 Pack

    TruForm

    FDA UDI
    Rmo, Inc.·00885797099822·MX 1/2 BI BD KT N/L R/L 170

    INFUSOR SV, INFUSOR LV, BAXTER PAIN MANAGEMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    FOTOMASTER

    FDA 510(k)
    FDA Class 2 ·Radiology

    NEUTRINO¿ NXT VR

    FDA Adverse Event
    Death ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWS·October 24, 2025

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·January 26, 2012

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·January 26, 2012

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC INC.·Product code KWP·October 15, 2009

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC INC.·Product code KWP·December 31, 2009

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC INC.·Product code KWP·October 29, 2009

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code LZG·February 13, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·March 1, 2011

    INTRAOCULAR LENS REXOOM RIGHT

    FDA Adverse Event
    Injury ·ADVANCED MEDICAL OPTICS·Product code HQL·February 22, 2008

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 21, 2010

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 21, 2010

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC INC.·Product code KWP·August 13, 2010

    ACS MULTI-LINK RX ULTRA CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·GUIDANT VASCULAR INTERVENTION·Product code MAF·October 25, 2006

    S/C TRIAL HANDLE ANGLED

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code HWA·September 23, 2019