BEUDAMED
    6 results · 42ms · Sources: EU EUDAMED, US FDA

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    Oculus Pentacam AXL Wave, Ref 70020, CE 0123

    FDA Recall
    Open, Classified ·Oculus Optikgeraete GMBH Munchholzhauser Str. 29 Wetzlar Germany·Product code MXK·August 8, 2023

    Pentacam HR REF 70900. Used to image the anterior segment of the eye.

    FDA Recall
    Open, Classified ·Oculus Optikgeraete GMBH Munchholzhauser Str. 29 Wetzlar Germany·Product code MXK·July 8, 2022

    Oculus Pentacam AXL , Ref 70100, CE 0123

    FDA Recall
    Open, Classified ·Oculus Optikgeraete GMBH Munchholzhauser Str. 29 Wetzlar Germany·Product code MXK·August 8, 2023

    Oculus Myopia Master , Ref 68100, CE 0123

    FDA Recall
    Open, Classified ·Oculus Optikgeraete GMBH Munchholzhauser Str. 29 Wetzlar Germany·Product code MXK·August 8, 2023

    Pentacam AXL Wave REF 70020. Used to image the anterior segment of the eye.

    FDA Recall
    Open, Classified ·Oculus Optikgeraete GMBH Munchholzhauser Str. 29 Wetzlar Germany·Product code MXK·July 8, 2022

    Pentacam AXL REF 70100, Pentacam HR REF 70900. Used to image the anterior segment of the eye.

    FDA Recall
    Open, Classified ·Oculus Optikgeraete GMBH Munchholzhauser Str. 29 Wetzlar Germany·Product code MXK·July 8, 2022