BEUDAMED
    26 results · 30ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    Paragon Adult Maxi PMP Oxygenator with Tubing Pack

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NA

    FDA UDI
    Synthes GmbH·10886982142207·2.4MM CORTEX SCREW SELF-TAPPING 12MM

    CODMAN

    FDA UDI
    Cerenovus, Inc.·10886704001416·CODMAN SLIM-LINE Aneurysm Clip Sideward Angled ...

    16PW - Washington Gas - Poly White

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588014425·16PW - Washington Gas - Poly White

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450854488·

    NYOrtho APEX CORE Wedge Pommel Wheelchair Cushion Gel-Foam 20x16x4x2

    FDA UDI
    N.Y. ORTHOPEDIC USA, INC.·00811677015842·For patients requiring hip positioning that are...

    NYOrtho APEX CORE Wedge Wheelchair Cushion Gel-Foam 20x16x4x2

    FDA UDI
    N.Y. ORTHOPEDIC USA, INC.·00811677015811·For patients that are inclined to slide forward...

    NYOrtho APEX CORE Wedge Pommel Wheelchair Cushion Gel-Foam 20x16x4x2

    FDA UDI
    N.Y. ORTHOPEDIC USA, INC.·00811677015835·For patients requiring hip positioning that are...

    SYNTHES CRANIOFACIAL PLATES

    FDA 510(k)
    FDA Class 2 ·Dental

    INSIGHT IMAGE GUIDED SURGICAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    SINGLE ACTION PUMPING SYSTEM CONTINUOUS FLOW

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KOD·January 20, 2025

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 27, 2014

    HS III PROXIMAL SEAL SYSTEM 3.8MM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·August 4, 2011

    PUMP, INFUSION, IMPLANTED, PROGRAMMABLE

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·July 2, 2013

    UNK - CONSTRUCTS: TOMOFIX PLATE/SCREWS

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HRS·September 29, 2021

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·December 20, 2023

    CEEON

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HQL·June 3, 2016

    CEEON

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HQL·June 3, 2016

    1.85MM TI MATRIX SCREW SELF-TAPPING/4MM

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code JEY·January 21, 2015

    VITROS XT 3400 CHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code JJE·July 13, 2020