BEUDAMED
    11 results · 21ms · 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 ×

    Mariner Pedicle Screw System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OCTARAY Mapping Catheter

    FDA UDI
    Biosense Webster Inc·10846835021110·OCTA,GALAXY,2-5-2-5-2,D-CURVE

    General Instruments

    FDA UDI
    ALPHATEC SPINE, INC.·00840180528853·Racetrack Cup Curette Size 02

    VENUS COMPOSITE

    FDA Adverse Event
    Malfunction ·HERAES KULZER GMBH·Product code EBF·December 23, 2013

    NORMAL SALINE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KPE·April 12, 2023

    STARCLOSE INTRODUCER SET MODEL- 1002

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AEDIS(TM)

    FDA 510(k)
    FDA Class 2 ·Dental

    QDOT MICRO

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code OAE·November 14, 2023

    CAPSUREFIX MRI SURESCAN

    FDA Adverse Event
    Injury ·MPRI·Product code NVN·October 10, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013

    KNIFE

    FDA Adverse Event
    Malfunction ·ALCON PRECISION DEVICE - SINKING SPRING·Product code HNN·June 16, 2011