BEUDAMED
    575 results · 24ms · 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 ×

    HandX Instrument - Monopolar Spatula

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    NA

    FDA UDI
    Stryker GmbH·00886385008776·Titanium Ankle Fusion Nail, Right

    EVOS Lumbar Interbody System

    FDA UDI
    Cutting Edge Spine, LLC·00841193100111·EVOS Straight HA PEEK 11mm x 9mm x 22mm Biconve...

    Altus Spine Interbody Fusion System

    FDA UDI
    Altus Spine, LLC·00843210131603·Broach Trial

    16PW - Class A 21 - Poly White

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588620114·16PW - Class A 21 - Poly White

    V.A.C. ABDOMINAL DRESSING

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

    NAVIGATION SOFTWARE HIP-UNIVERSAL; NAVIGATION SOFTWARE HIP THR-AESCULAP

    FDA 510(k)
    FDA Class 2 ·Neurology

    PRECURVED PALINDROME EMERALD 19/36KIT

    FDA Adverse Event
    Other ·COVIDIEN·Product code MSD·March 22, 2011

    OPTI-FREE UNSPECIFIED PRODUCT

    FDA Adverse Event
    Injury ·ALCON - FORT WORTH / ALCON LABORATORIES, INC.·Product code LPN·March 31, 2011

    HEARTSTART 4000

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE - ANDOVER·Product code MKJ·September 1, 2011

    AMBIT PCA MILITARY PUMP/CASSETTE FILTER MALE

    FDA Adverse Event
    Death ·SUMMIT MEDICAL PRODUCTS, INC.·Product code MEA·October 21, 2011

    ASR ACETABULAR CUPS 50

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD.·Product code KWA·June 25, 2014

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MFK·August 19, 2011

    ALLURA XPER FD10/10

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code IZI·February 18, 2011

    MODULAR ANALYTICS CORE

    FDA Adverse Event
    Injury ·HITACHI HIGH TECH. CORP.·Product code JJE·November 6, 2008

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORP·Product code MKJ·August 17, 2011

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·July 5, 2013

    OPTI-FREE REPLENISH

    FDA Adverse Event
    Injury ·ALCON - FORT WORTH / ALCON LABS, INC.·Product code LPN·July 27, 2011

    CAPSURE SP

    FDA Adverse Event
    Malfunction ·MEDTRONIC·Product code DTB·August 12, 2023

    BV PULSERA, REL. 2.3

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code IZL·February 18, 2011