BEUDAMED
    45 results · 23ms · Sources: EU EUDAMED, US FDA

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    Xario 200 Diagnostic Ultrasound System V5.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    ZEUS-L

    FDA UDI
    SPINAL ELEMENTS·00840916140977·ZEUS® LLIF 16mm x 21mm x 55mm x 07° TRIAL

    ZEUS-L

    FDA UDI
    SPINAL ELEMENTS·00840916141080·ZEUS® LLIF 16mm x 21mm x 55mm x 28° TRIAL

    ZEUS-L

    FDA UDI
    SPINAL ELEMENTS·00840916120535·ZEUS®-L Hyper, 16 x 21 x 55mm, 21 degrees

    ZEUS-L

    FDA UDI
    SPINAL ELEMENTS·00840916134273·ZEUS®-L, Lateral Lumber Interbody Fusion Device...

    ZEUS-L

    FDA UDI
    SPINAL ELEMENTS·00840916141066·ZEUS® LLIF 16mm x 21mm x 55mm x 21° TRIAL

    ZEUS-L

    FDA UDI
    SPINAL ELEMENTS·00840916134310·ZEUS®-L, Lateral Lumber Interbody Fusion Device...

    ZEUS-L

    FDA UDI
    SPINAL ELEMENTS·00840916120528·Hyper ZEUS®-L 16 x 21 x 55mm, 14 Degree

    ZEUS-L

    FDA UDI
    SPINAL ELEMENTS·00840916141028·ZEUS® LLIF 16mm x 21mm x 55mm x 14° TRIAL

    MR RADIATION ONCOLOGY OPTIONS

    FDA 510(k)
    FDA Class 2 ·Radiology

    DIGITAL MXR-D FLOWMETER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOB·July 27, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOB·October 26, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOB·July 24, 2021

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 3, 2017

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOB·May 28, 2024

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOB·October 14, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOB·April 19, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOB·October 14, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOB·September 14, 2022