BEUDAMED
    94 results · 23ms · Sources: EU EUDAMED, US FDA

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    Stent, Carotid

    FDA Pre-Market Approval
    FDA Class 3 ·CGuard Prime Carotid Stent System

    Stent, Carotid

    FDA Pre-Market Approval
    FDA Class 3 ·CGuard™ Prime Carotid Stent System

    Stent, Carotid

    FDA Pre-Market Approval
    FDA Class 3 ·CGuard™ Prime Carotid Stent System

    MaXcess

    FDA UDI
    Nuvasive, Inc.·00887517196187·MaXcess 4 Retractor, Wide Anterior Long

    PILLING

    FDA UDI
    TELEFLEX INCORPORATED·14026704799241·

    4.0 / 5.2mm DOUBLE DRILL GUIDE

    FDA UDI
    Osteocentric Technologies, Inc.·00810189110564·4.0 / 5.2mm DOUBLE DRILL GUIDE

    BD SAF-T-INTIMA IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS·Product code FOZ·April 17, 2007

    Zio AT® device (A100A1001)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD SAF-T-INTIMA IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS·Product code FOZ·April 17, 2007

    BD SAF-T-INTIMA IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEM·Product code FOZ·April 17, 2007

    BD SAF-T-INTIMA IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS·Product code FOZ·April 17, 2007

    BD SAF-T-INTIMA IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS·Product code FOZ·April 17, 2007

    BD SAF-T-INTIMA IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS·Product code FOZ·April 17, 2007

    BD INSULIN SYRINGES

    FDA Adverse Event
    Injury ·BECTON DICKINSON AND COMPANY·Product code FMF·April 17, 2025

    Covidien Auto Suture" Blunt Tip Trocar, Product Number OMS-T10BTNL

    FDA Enforcement
    Class II ·Ongoing·Covidien, LP·April 10, 2024

    Lens, Contact, Orthokeratology, Overnight

    FDA Pre-Market Approval
    FDA Class 3 ·Euclid Orthokeratology (oprifocon A) Contact Lenses for Overnight Wear and Euclid Orthokeratology (tisilfocon A) Contact

    Implant, Dermal, For Aesthetic Use

    FDA Pre-Market Approval
    FDA Class 3 ·Restylane Refyne, Restylane Defyne

    INTELLIVUE MULTI MEASUREMENT SERVER X2

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·May 28, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·September 8, 2011

    ENERGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 22, 2013