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

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    Digital Blood Pressure Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Unity Total Knee System

    FDA UDI
    CORIN LTD·05056139232879·Patella Caliper

    BD BBL™ Sensi-Disc™ Minocycline 30 µg

    FDA UDI
    BECTON, DICKINSON AND COMPANY·00382902312505·BD BBL™ Sensi-Disc™ Minocycline 30 µg

    VK Couture

    FDA UDI
    Diversified Products, Inc.·00842894182192·

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111160219·SKLARLT SKLARCT RAGNELL CVD 5"

    Rx Knee Femoral Cone Augment Reamer Size Small

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215147815·

    Regatta Lateral System

    FDA UDI
    Seaspine Orthopedics Corporation·10889981158965·Lateral Implant, 23mm x 12mm x 50mm, 10 Deg

    Regatta Lateral System

    FDA UDI
    Seaspine Orthopedics Corporation·10889981158972·Lateral Implant, 23mm x 12mm x 50mm, 15 Deg

    Regatta Lateral System

    FDA UDI
    Seaspine Orthopedics Corporation·10889981158958·Lateral Implant, 23mm x 12mm x 50mm, 0 Deg

    DBC PRESS ACUPUNCTURE NEEDLES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TIGER SPINE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DRILL, AO, STERILE 4, 2X340 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·September 23, 2011

    Vu aPod™ - L

    FDA UDI
    Seaspine Orthopedics Corporation·10889981046705·LATERAL IMPLANT, LORDOTIC, 12mm X 23mm X 50mm X...

    OPTILITE® FREELITE® KAPPA FREE KIT

    FDA Adverse Event
    Injury ·THE BINDING SITE LIMITED·Product code DFH·March 30, 2026

    OPTILITE® FREELITE® KAPPA FREE KIT

    FDA Adverse Event
    Injury ·THE BINDING SITE LIMITED·Product code DFH·March 31, 2026

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·November 4, 2022

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·December 21, 2020

    GE OEC 9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·November 13, 2008

    4.0MM 90-S MAX SERFAS ENERGY SUCTION PROBE

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY PUERTO RICO·Product code GEI·July 25, 2011

    ARTICULEZE M HEAD 36MM +5

    FDA Adverse Event
    Injury ·8010379 DEPUY INTL., LTD.·Product code JDI·July 17, 2013