BEUDAMED
    352 results · 29ms · Sources: EU EUDAMED, US FDA

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    ULTHERA SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    NexxZr™ T / D-100-20-NT-A300-SD

    FDA UDI
    SAGEMAX BIOCERAMICS, INC·00842271112385·

    MEGA PLUS SPINE SYSTEM

    FDA UDI
    BK MEDITECH CO.,LTD.·08809665580252·Rod(CoCr), Ø6.0 x 280mm

    SI-LOK SACROILIAC JOINT FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NEOTRACT ANCHOR SYSTEM MODEL TAS400

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Injury ·PENTAX·Product code EOQ·January 10, 2017

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·December 27, 2021

    INTRALASE FS2

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HNO·May 29, 2013

    TAPER FIT

    FDA Adverse Event
    Injury ·CORIN LTD.·Product code LZO·September 26, 2014

    ASKU

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA INC.·Product code DTE·June 16, 2011

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·October 15, 2021

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·June 17, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FAJ·December 27, 2021