BEUDAMED
    13 results · 20ms · 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 ×

    MULTISLICE UPGRADE KIT FOR AQUILION CT SCANNER, TSX-101A (AQUILION,MULTI)

    FDA 510(k)
    FDA Class 2 ·Radiology

    CT40

    FDA UDI
    SUNTECH MEDICAL, INC.·10840935106029·

    CT40

    FDA UDI
    SUNTECH MEDICAL, INC.·10840935106821·

    CT40

    FDA UDI
    SUNTECH MEDICAL, INC.·10840935106005·

    CT40

    FDA UDI
    SUNTECH MEDICAL, INC.·10840935106135·

    CT40

    FDA UDI
    SUNTECH MEDICAL, INC.·10840935106012·

    INTRAVENOUS POWER INJECTOR EXTENSION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Full Automatic (NIBP) Blood Pressure Monitor-HL158TB

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PULSE GEN MODEL 103

    FDA Adverse Event
    Injury ·CYBERONICS INC·Product code LYJ·March 5, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011

    CONCERTO II CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·August 7, 2014

    UNKNOWN

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·June 9, 2021

    ZIMMON PANCREATIC STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·October 16, 2020