BEUDAMED
    7 results · 19ms · 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 ×

    BLOOD TRANSFUSION SET (SANGOFIX)

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    NexxZr Plus Multi 2.0 A2 W98-20mm

    FDA UDI
    SAGEMAX BIOCERAMICS, INC·00842271158604·

    ALLIENT SORBET HEMODIALYSIS SYSTEM, MODEL 1100

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

    TE7 Diagnostic Ultrasound System

    FDA 510(k)
    FDA Class 2 ·Radiology

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·April 21, 2014

    ENDO STITCH 10MM SUTURING DEVICE

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY US·Product code KOG·September 18, 2012

    ACCU-CHEK ® PERFORMA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·July 19, 2010