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

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    Dual Lumen Ureteral Access Catheter, Flexi-Tip Dual Lumen Ureteral Access Catheter

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Maestro™ Total Wrist

    FDA UDI
    Biomet Orthopedics, LLC·00887868239564·

    MAESTRO TOTAL WRIST

    FDA UDI
    Biomet Orthopedics, LLC·00880304439078·

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780181507·Integra® Jarit® Laparatomy Ring, 1-1/2"

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014614·PedFuse Respond, SLD, 6.0mm x 35mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014652·Ø6.0mmX55mm Solid Respond Screw Assy

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014645·PedFuse Respond, SLD, 6.0mm x 50mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014638·PedFuse Respond, SLD, 6.0mm x 45mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014607·PedFuse Respond, SLD, 6.0mm x 30mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361014621·PedFuse Respond, SLD, 6.0mm x 40mm

    ZENO PMMA DISC

    FDA 510(k)
    FDA Class 2 ·Dental

    SALVIN DENTAL SPECIALTIES FIXATION SCREW

    FDA 510(k)
    FDA Class 2 ·Dental

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·July 19, 2023

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·September 6, 2022

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·March 14, 2023

    FIXED LOCKING SCREW 4.75MMX15MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWJ·February 2, 2017

    INSTINCT JAVA BLOCKER

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code NKB·June 13, 2013

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·July 27, 2011

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·September 29, 2008

    ARTHREX ANGEL SYSTEM WITH ASPIRATION KIT

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code ORG·May 1, 2019