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

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    Dexcom G6 Continuous Glucose Monitoring (CGM) System

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517578310·CoRoent Ant TLIF Ti 10x11x32mm 8°

    FAA Airline - 24 Poly White

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588013244·FAA Airline - 24 Poly White

    FAA Airline - 24 Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588013237·FAA Airline - 24 Metal

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450157077·

    INTRODUCER SHEATH

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

    SMART BAG MO

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ENDOBON XENOGRAFT GRANULES

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LYC·February 21, 2017

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·October 27, 2020

    ENDOBON GRANULES

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code LYC·February 20, 2017

    PRECISION SPECTRA®

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 27, 2014

    TERUMO VIRTUOSAPH VEIN HARVESTING SYSTEM

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code GCJ·August 3, 2011

    ALAIR BRONCHIAL THERMOPLASTY CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - SAN JOSE·Product code OOY·July 2, 2013

    I-STAT PT/INRCARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code GJS·November 18, 2013

    TOTAL ASR ACET IMP SIZE 58

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·July 10, 2013

    DEPUY ASR XL FEM IMP SIZE 51

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·July 10, 2013

    CORAIL2 NON COL HO SIZE 14

    FDA Adverse Event
    Injury ·DEPUY FRANCE SAS-3003895575·Product code KWA·May 13, 2015

    HABIB ENDOHPB

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·January 30, 2023

    HANCOCK II AORTIC 23MM

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·March 18, 2014

    UNKNOWN_SPINE_PRODUCT

    FDA Adverse Event
    Malfunction ·STRYKER SPINE-US·Product code NKB·May 9, 2024