BEUDAMED
    87 results · 23ms · Sources: EU EUDAMED, US FDA

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    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·CUSTOMFLEX CONTACT LENS

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·TRIPOL 43

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·CUSTOMFLEX (DELTAFILCON A) HYDROPHILIC CONTACT LEN

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·CUSTOMFLEX CONTACT LENS

    Transport Endoscopic Access Device

    FDA UDI
    Usgi Medical, Inc.·00860009064706·Transport Endoscopic Access Device

    Proficient™ Posterior Cervical Spine System

    FDA UDI
    Spine Wave, Inc.·10840642113426·Extended Tab Screw, 5.5 mm x 44 mm

    3M™ Unitek™

    FDA UDI
    3M UNITEK CORPORATION·00652221049193·Unitek(TM) Blue Flexiloy 14 in. Straight Length...

    DRESSER ARGUS P/N 1818

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Camaro Support Catheter

    FDA UDI
    QXMEDICAL·00853892004195·Support Catheter, 180 cm working length, compat...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197044998·Tissue Forceps 1x2 te...

    SURGICOUNT

    FDA UDI
    STRYKER CORPORATION·57613327512743·+ SAFE-T-Lap Sponge, 18 inch x 18 inch, RFID, ...

    SURGICOUNT

    FDA UDI
    STRYKER CORPORATION·37613327512817·+ SAFE-T-Lap Sponge, 18 inch x 18 inch, RFID, ...

    SURGICOUNT

    FDA UDI
    STRYKER CORPORATION·37613327512800·+ SAFE-T-Lap Sponge, 18 inch x 18 inch, RFID, X...

    SURGICOUNT

    FDA UDI
    STRYKER CORPORATION·37613327512831·+ SAFE-T-Lap Sponge, 18 inch x 18 inch, RFID, X...

    SURGICOUNT

    FDA UDI
    STRYKER CORPORATION·57613327512712·+ SAFE-T-Lap Sponge, 18 inch x 18 inch, RFID, X...

    SURGICOUNT

    FDA UDI
    STRYKER CORPORATION·57613327512767·+ SAFE-T-Lap Sponge, 18 inch x 18 inch, RFID, X...

    PLATINUM PLUS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQX·March 5, 2019

    ONE TOUCH ULTRA

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·September 20, 2002

    ONE TOUCH BASIC ENHANCED

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·August 23, 2002

    ONE TOUCH ULTRA

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·September 23, 2002