BEUDAMED
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    GenX-CR

    FDA 510(k)
    FDA Class 2 ·Dental

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112939·CORNEAL TREPHINE BLADE8.0MM

    BD INSULIN SYRINGE

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·May 14, 2021

    XIVE DENTAL IMPLANT SYSTEM MULTIPLE

    FDA 510(k)
    FDA Class 2 ·Dental

    NOVOHIP TOTAL HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ONE TOUCH BASIC

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·May 6, 2003

    ONE TOUCH ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code NBW·November 4, 2008

    UNICEL® DXH 800 COULTER® CELLULAR ANALYSIS SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·September 2, 2011

    LINOX S 65

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code NVY·July 17, 2013

    SYRINGE 1.0ML 31GA 8MM 10BAG 500 PL/WG

    FDA Adverse Event
    Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·February 18, 2021