BEUDAMED
    15 results · 32ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    ACE CLINICAL CHEMISTRY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Couture Essence

    FDA UDI
    Carolon Company·00078301930142·

    Novo Surgical

    FDA UDI
    NOVO SURGICAL, INC.·00842331115585·Maxi-Type Grasping Forceps - Double Curved, 5.0...

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867059955·ECLIPSE CAGE SCREW XL, 45MM

    PRIME ECG SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GUIDEWIRE, PURSUER SERIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·January 25, 2013

    GENESIS II

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC., BROOKS MANUFACTURING SITE·Product code JWH·December 16, 2010

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 11, 2014

    UNI GLENOID-PERIPHERAL LOCK SCRW

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·July 26, 2024

    ECLIPSE TRUNION,45 MM TPS CTD

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code QHQ·July 26, 2024

    CENTRAL SCREW, NL, UNI REV, 6.5X25MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·July 26, 2024

    ECLIPSE CAGE SCREW XL, 45MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code QHQ·July 26, 2024

    UNIVERSAL GLENOID - INLAY LARGE

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·July 26, 2024

    UNIVERSAL GLENOID - BASEPLATE LARGE

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·July 26, 2024