BEUDAMED
    7 results · 24ms · 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 Status: Completed ×

    Medtronic SynchroMed, Model A10

    FDA Enforcement
    Class II ·Completed·Medtronic Inc.·December 20, 2023

    Protege GPS Self-Expanding Peripheral Stent System, product number SERB65-09-60-80, Sterile.

    FDA Enforcement
    Class II ·Completed·Medtronic Inc.·January 10, 2024

    Medtronic SynchroMed, Model A10

    FDA Recall
    Completed ·Medtronic Inc.·Product code LKK·July 13, 2020

    Protege GPS Self-Expanding Peripheral Stent System, product number SERB65-09-60-80, Sterile.

    FDA Recall
    Completed ·Medtronic Inc.·Product code NIP·November 20, 2023

    Medical Device Identification Cards associated with Sprint Quattro Lead, Product/CFN 6935M72

    FDA Recall
    Completed ·Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)·Product code NVY·November 8, 2021

    Medical Device Identification Cards associated with Astra XT DR Implantable pulse generator

    FDA Recall
    Completed ·Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)·Product code NVZ·November 8, 2021

    LINQ II Insertable Cardiac Monitor

    FDA Recall
    Completed ·Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)·Product code MXD·January 18, 2022