BEUDAMED
    56 results · 22ms · 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 ×

    Dr. Amplatz Micro Plug

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172971390·

    CORELEADER HEMO-PAD MODEL CPII 02030

    FDA 510(k)
    FDA Unclassified ·Unknown

    CRYSTALSERT CRYSTALENS DELIVERY SYSTEM

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    NIPRO BLOOD TUBING SET W/TP

    FDA Adverse Event
    Malfunction ·NIPRO (THAILAND) CORP. LTD.·Product code FJK·February 6, 2024

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 6, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 4, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021