BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

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    ENDOMET

    FDA 510(k)
    FDA Class 2 ·Dental

    Lancer Gear

    FDA UDI
    LANCER ORTHODONTICS, INC.·00817573023851·CERVICAL"LANCER GEAR"BLACK/PURPLE 5/PK

    NETWORK EYE SPEARS, POINTS, DRAINS, WICKS AND SHIELDS

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    ENHANCE SPERM FREEZE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    INFINITI VISION SYSTEM

    FDA Adverse Event
    Injury ·ALCON - IRVINE TECHNOLOGY CTR·Product code HQC·May 1, 2014

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·November 13, 2012

    ACCU-CHEK ® COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·September 10, 2010

    4.2MM THREE-FLUTED DRILL BIT QC/NEEDLE POINT/145MM

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HTW·August 31, 2021

    DRILL BIT Ø4.2 CALIBR L145 3FLUTE F/QUIC

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTW·March 22, 2024