BEUDAMED
    20 results · 21ms · 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 ×

    Healgen URS Test Strips

    FDA 510(k)
    FDA Class 1 ·Hematology

    Unity Total Knee System

    FDA UDI
    CORIN LTD·05056139233715·Extraction Tool

    Proxis™ Ureteral Access Sheath

    FDA UDI
    C. R. Bard, Inc.·00801741101694·Proxis™ Ureteral Access Sheath

    DVX5.5 SPINE SYSTEM

    FDA UDI
    BK MEDITECH CO.,LTD.·08809228126644·Cross-Link, 45mm

    MEGA5.5 SPINE SYSTEM

    FDA UDI
    BK MEDITECH CO.,LTD.·08809228126088·Cross-Link, 45mm

    Symmetry Surgical

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482001325·Symmetry® Curette, Spinal, Straight, Size 2, 8 ...

    MILLENNIUM

    FDA UDI
    Avalign Technologies, Inc.·00190776291679·Spinal Fusion Curette, size 2

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180158627·CANNULA 4.5 IRRIG CANNULA

    Regatta Lateral System

    FDA UDI
    Seaspine Orthopedics Corporation·10889981158828·Lateral Implant, 23mm x 10mm x 45mm, 10 Deg

    Regatta Lateral System

    FDA UDI
    Seaspine Orthopedics Corporation·10889981162115·Lateral Implant, 23mm x 10mm x 45mm, 15 Deg

    Regatta Lateral System

    FDA UDI
    Seaspine Orthopedics Corporation·10889981158811·Lateral Implant, 23mm x 10mm x 45mm, 0 Deg

    ENTERPRISE ECG ANALYSIS / INTERPRETATION SOFTWARE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AEROLET TOILET LIFT, MODEL AER-01

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Vu aPod™ - L

    FDA UDI
    Seaspine Orthopedics Corporation·10889981046644·LATERAL IMPLANT, WIDE, LORDOTIC, 10mm X 23mm X ...

    BRAVO

    FDA Adverse Event
    Malfunction ·ARIZONA DEVICE MANUFACTURING·Product code FFT·October 30, 2008

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code MDS·July 19, 2011

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 12, 2013

    S5 CONSOLE FOR 4 PUMP

    FDA Adverse Event
    Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DWA·December 16, 2016

    S5 ROLLER PUMP

    FDA Adverse Event
    Malfunction ·LIVANOVA DEUTSCHLAND·Product code DWB·October 3, 2016

    PROXIS¿ URETERAL ACCESS SHEATH

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (COVINGTON) -1018233·Product code FED·April 14, 2025