BEUDAMED
    25 results · 29ms · Sources: EU EUDAMED, US FDA

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    Ophthalmic Knife

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113356·CLEAR CORNEA KNIFE 2.8MM (BX/5)

    NOBELACTIVE TIULTRA NP 3.5X13MM

    FDA Adverse Event
    Injury ·NOBEL BIOCARE AB·Product code DZE·May 31, 2021

    NOBELACTIVE TIULTRA NP 3.5X13MM

    FDA Adverse Event
    Injury ·NOBEL BIOCARE AB·Product code DZE·May 31, 2021

    TiUltra Implants and Xeal Abutments

    FDA 510(k)
    FDA Class 2 ·Dental

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517568748·CoRoent Ant TLIF Ti, 10x12x34mm 4°

    24PW - Hanta Virus

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588013442·Hanta Virus - 24 Poly White

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523144402·CIMA HXL Domed Patella Sz 3 34mm 9.0mm Thick

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523144396·CIMA HXL Domed Patella Sz 2 30mm 8.5mm Thick

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523144419·CIMA HXL Domed Patella Sz 4 38mm 9.5mm Thick

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523144426·CIMA HXL Domed Patella Sz 5 42mm 10.0mm Thick

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523144389·CIMA HXL Domed Patella Sz 1 27mm 8.0mm Thick

    MDIXON SOFTWARE OPTION FOR INTERA 1.5T, ACHIEVA 1.5T & ACHIEVA 3.0T MR SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Radiology

    TRINICA SELECT ANTERIOR CERVICAL PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD BBL¿ TRYPTICASE SOY AGAR WITH 5% SHEEP BLOOD (TSA II)

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JSG·November 19, 2022

    CAPIO BULLET SUTURES

    FDA Adverse Event
    Malfunction ·TELEFLEX·Product code GAW·October 10, 2008

    URETEX SUPPORT PP KIT Z1

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code OTN·June 21, 2013

    ASR UNI FEMORAL IMPL SIZE 45

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·August 8, 2011

    WATCHMAN FLX PRO LAA CLOSURE DEVICE WITH DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NGV·December 19, 2023

    AXIOS STENT AND ELECTROCAUTERY ENHANCED DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code PCU·August 21, 2024

    MEDTRONIC CRT

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code NIK·December 12, 2023