BEUDAMED
    6 results · 13ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Open, Classified ×

    CoolCurve+ ZELTIQ Vacuum Applicator REF BRZ-AP1-064-000

    FDA Recall
    Open, Classified ·Zeltiq Aesthetics, Inc·Product code OOK·June 9, 2022

    CoolFit ZELTIQ Vacuum Applicator REF BRZ-AP1-066-000

    FDA Recall
    Open, Classified ·Zeltiq Aesthetics, Inc·Product code OOK·June 9, 2022

    CoolCurve ZELTIQ Vaccum Applicator REF BRZ-AP1-062-000

    FDA Recall
    Open, Classified ·Zeltiq Aesthetics, Inc·Product code OOK·June 9, 2022

    CoolMax ZELTIQ Vacuum Applicator REF BRZ-AP1-080-000

    FDA Recall
    Open, Classified ·Zeltiq Aesthetics, Inc·Product code OOK·June 9, 2022

    CoolCore ZELTIQ Vacuum Applicator REF BRZ-AP1-063-000

    FDA Recall
    Open, Classified ·Zeltiq Aesthetics, Inc·Product code OOK·June 9, 2022

    XEN Gel Stent, REF 5513-001(US Model), Sterile, RX Only, (01)10888628032439 ; Other Model Numbers: 5507-001(Global Model) and 5517-001(Australia model) Implant for glaucoma treatment.

    FDA Recall
    Open, Classified ·Allergan PLC·Product code KYF·October 30, 2019