BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    Invisalign System

    FDA 510(k)
    FDA Class 2 ·Dental

    Ophthalmic Knife

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113240·VITRECTOMY KNIFE 23GA (BX/5)

    DENTITION INTEGRATING MATERIAL

    FDA 510(k)
    FDA Class 2 ·Dental

    TROJAN MAGNUM CONDOM WITH FIRE & ICE LUBRICANT

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

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 30, 2024

    POLARCATH

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code DQY·November 3, 2008

    TRILOGY CROSSLINKED POLYETHYLENE LINER

    FDA Adverse Event
    Injury ·ZIMMER·Product code LPH·August 16, 2011

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·July 11, 2013

    TI TOMOFIX MEDIAL HIGH TIB PL LT/ANAT/4 HOLES/112MM/STER

    FDA Adverse Event
    Injury ·OBERDORF : SYNTHES PRODUKTIONS GMBH·Product code HRS·October 8, 2018