BEUDAMED
    21 results · 21ms · Sources: EU EUDAMED, US FDA

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    Journey II Unicompartmental Knee System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ATLANTIS® Anterior Cervical Plate System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994235787·PLATE 6190085 ANTERIOR CERVICAL 85MM

    ATLANTIS® Anterior Cervical Plate System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00763000868024·PLATE 6190085 ANTERIOR CERVICAL 85MM

    Jawz Endomyocardial Biopsy Forceps

    FDA UDI
    ARGON MEDICAL DEVICES, INC.·00886333206834·Jawz Endomyocardial Biopsy Forceps 7F x 105cm S...

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690196327·AK3 PS Instruments Pan

    N/A

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K190055001·MTM® NO TRACE (TM) 018 UL/4-4

    IN-OVATION® L

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K190055011·IN-OVATION® L 018 UPPER 6-6

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690195016·AK3 PS Instruments Pan Insert

    IN-OVATION® L

    FDA UDI
    DENTSPLY SIRONA ORTHODONTICS INC.·D807K190055101·IN-OVATION® L 018 UL/7-7

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306821783·Laryngeal Mirror #5

    Mariner Cortical

    FDA UDI
    Seaspine Orthopedics Corporation·10889987169521·CORTICAL SHANK, Cannulated, 9.0 X 85

    Mariner Cortical

    FDA UDI
    Seaspine Orthopedics Corporation·10889981169527·CORTICAL SHANK, Cannulated, 9.0 X 85

    MERCI RETRIEVER, MODELS 90050, 90060, 90066, 90070, 90110, 90111, 90112, 90113

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VANTAGE VIEW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Coral

    FDA UDI
    Seaspine Orthopedics Corporation·10889981027599·Prebent Rod 5.5 x 85. The Coral Spinal System c...

    UNKNOWN_NEUROVASCULAR_PRODUCT

    FDA Adverse Event
    Injury ·CONCENTRIC MEDICAL·Product code NRY·December 14, 2012

    MCLEAN-RING NASOJEJUNAL FEEDING TUBE SET

    FDA Adverse Event
    Injury ·COOK INC·Product code KNT·November 10, 2021

    IDENTITY XL DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·January 11, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 18, 2013

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC·Product code GJS·June 29, 2011