BEUDAMED
    9 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 ×

    Rhinolaryngoscope system

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    SMITH & NEPHEW GLOBAL FEMORAL HEAD TRIALS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Comprehensive Humeral Fracture Positioning Sleeves

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PIPELINE EMBOLIZATION DEVICE

    FDA Adverse Event
    Injury ·COVIDIEN·Product code OUT·November 6, 2014

    SYNCHRON® LX20 ANALYZER (W/O CAP PIERCER)

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·September 2, 2011

    GYNECARE PROLIFT +M POSTERIOR PELVIC FLOOR REPAIR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTP·July 18, 2013

    BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAIVED KIT

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·February 9, 2026

    BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAIVED KIT

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·February 10, 2026

    BD VERITOR¿ PLUS ANALYZER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code PSZ·March 7, 2025