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 ×

    Corvocet Coaxial Introducer

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

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100226·THORLAKSON ASPIRATING SPECULUM

    EMBRACE

    FDA 510(k)
    FDA Class 2 ·Radiology

    CRONUS GUIDEWIRE, MODEL 001-001470-1

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    7700

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·May 30, 2013

    12/14 ARTICUL 40MM M SPEC+8.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LPH·June 30, 2011

    PALMAZ GENESIS OPTA PRO

    FDA Adverse Event
    Injury ·CORDIS EUROPA, N.V.·Product code FGE·May 22, 2008

    SOLITAIRE

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code NRY·January 11, 2024

    Medical Linear Accelerator

    FDA Enforcement
    Class II ·Terminated·Elekta, Inc.·September 14, 2016

    Veradius Unity with Software Release 2.1- Amobile, diagnostic X-ray imaging and viewing system. . Model Number: 718132

    FDA Enforcement
    Class II ·Ongoing·Philips North America Llc·December 15, 2021