BEUDAMED
    13 results · 20ms · 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 ×

    Microwave Ablation Antennas

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Guerbet

    FDA UDI
    Shenzhen Boon Medical Supply Co., Ltd.·06938327906900·12h CT 200ml Syringe(Green)

    Ormco

    FDA UDI
    ORMCO CORPORATION·00889989074833·TUBE RECT SOFT 18X25X2MM 2-1011

    Meridian

    FDA UDI
    Seaspine Orthopedics Corporation·10889981247591·No-Profile Interbody, 43mm x 30mm x 18mm, 25 Deg

    IDEAL Locking Plate System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SMITH & NEPHEW GENESIS II DEEP FLEXION CRUCIATE RETAINING ARTICULAR INSERT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·September 20, 2024

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·November 10, 2014

    1423500-2011-11984

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·September 9, 2011

    UNICEL® DXC 600I SYNCHRON® ACCESS® CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code JJE·July 22, 2013

    ARCOS 17X150MM SPL TPR DIST

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·June 12, 2024

    ARCOS CON SZ C STD 60MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·June 12, 2024

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·April 15, 2015