BEUDAMED
    10 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 ×

    FLEXIBLE MINI-FIBERSCOPES

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

    X-CORE

    FDA UDI
    Nuvasive, Inc.·00887517269904·X-CORE Mini Core, Ø12mm 17-24mm

    FETCH ASPIRATION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EBit Series Diagnostic Ultrasound System

    FDA 510(k)
    FDA Class 2 ·Radiology

    SCREW,FIXATION,BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·July 11, 2016

    LD304 MATERNITY BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code HDD·February 14, 2013

    LIGAMAX-5MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·January 17, 2011

    S-ROM*STM STD,42 NK,18X13X160

    FDA Adverse Event
    Malfunction ·DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDICS - 1219·Product code JDI·July 28, 2014

    Daig Livewire Steerable, Product Number 401932; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026

    Exactech Equinoxe REVERSE SHOULDER,38mm Constrained Humeral Liner: a) +0mm, Item Number 320-38-10, b) +2.5mm, Item Number 320-38-13, Shoulder Arthroplasty

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·April 10, 2024