BEUDAMED
    42 results · 21ms · Sources: EU EUDAMED, US FDA

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    ZIMMER PATIENT SPECIFIC INSTRUMENTS SYSTEM, ZIMMER PATIENT SPECIFIC INSTRUMENTS, ZIMMER PATIENT SPECIFIC INSTRUMENTS PLA

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Castroviejo Keratoplasty and Keratectomy Scissors

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896112186·Castroviejo Keratoplasty and Keratectomy Scisso...

    ELECSYS PTH CALCHECK 5

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    LINICAL CHEMISTRY CALIBRATION VERIFIERS LEVELS A-E FOR OLYMPUS AU SYSTEMS

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    CUSTOM JTS NON-INVASIVE DISTAL FEMUR IMPLANT

    FDA Adverse Event
    Injury ·STANMORE IMPLANTS WORLDWIDE LTD.·Product code LWJ·May 15, 2015

    CUSTOM JTS NON-INVASIVE DISTAL FEMUR IMPLANT

    FDA Adverse Event
    Malfunction ·STANMORE IMPLANTS WORLDWIDE LTD.·Product code KRO·December 24, 2014

    CUSTOM JTS NON-INVASIVE DISTAL FEMUR IMPLANT

    FDA Adverse Event
    Malfunction ·STANMORE IMPLANTS WORLDWIDE LTD.·Product code KRO·December 23, 2014

    M.U.S.T. PEDICLE SCREW 7X45

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MNI·January 20, 2017

    CUSTOM PROXIMAL TIBIA JTS

    FDA Adverse Event
    Malfunction ·STANMORE IMPLANTS WORLDWIDE LTD·Product code KRO·December 24, 2014

    CUSTOM JTS NON-INVASIVE DISTAL FEMUR IMPLANT

    FDA Adverse Event
    Malfunction ·STANMORE IMPLANTS WORLDWIDE LTD.·Product code KRO·December 24, 2014

    PRECISION®

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·May 29, 2013

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 19, 2011

    XACT CAROTID STENT SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR GALWAY·Product code NIM·August 22, 2008

    PEDICLE SCREW 03.50.030 PEDICLE SCREW 7X40

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·February 3, 2020

    JTS DRIVE UNIT FOR CUSTOM JTS NON-INVASIVE DISTAL FEMUR IMPLANT

    FDA Adverse Event
    Malfunction ·STANMORE IMPLANTS WORLDWIDE LTD·Product code KRO·December 24, 2014

    MECTALIF POSTERIOR

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·October 8, 2025

    JTS EXTENDIBLE DISTAL FEMUR IMPLANT

    FDA Adverse Event
    Malfunction ·STANMORE IMPLANTS WORLDWIDE LTD·Product code KRO·December 23, 2014

    DISTAL FEMUR MINIMALLY INVASIVE GROWER (MIG)

    FDA Adverse Event
    Malfunction ·STANMORE IMPLANTS WORLDWIDE LTD·Product code KRO·February 11, 2015

    CUSTOM DISTAL FEMUR JTS REPLACEMENT IMPLANT

    FDA Adverse Event
    Malfunction ·STANMORE IMPLANTS WORLDWIDE LTD·Product code KRO·April 10, 2015

    MECTALIF OBLIQUE INTERBODY FUSION DEVICE PEEK/TI 12X28X7 L0°

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code MAX·November 10, 2017