BEUDAMED
    9 results · 23ms · 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.

    I.V. START KITS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Ultraverse® 018

    FDA UDI
    Bard Peripheral Vascular, Inc.·00801741054730·Ultraverse® 018 PTA Balloon Dilatation Catheter...

    Medtronic Reusable Instruments

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00673978069579·INSTRUMENT 875-315 CURETTE ANGLED 1 0

    WHITE PLUME ABSORBENT BANDAGE

    FDA 510(k)

    ORAL ASPIRATOR

    FDA 510(k)
    FDA Class 1 ·Dental

    UNIDENTIFIED HIP IMPLANTENDURON LINER 44¿OD-22¿ID

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·June 16, 2014

    CAPSUREFIX

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 19, 2010

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·December 17, 2012

    MIDWEST ENERGO 1:5

    FDA Adverse Event
    Malfunction ·SIRONA DENTAL SYSTEMS GMBH·Product code EFB·April 23, 2026