BEUDAMED
    8 results · 17ms · 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.

    ACUMASTER BRAND ACUPUNCTURE NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NONE

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code UNK·December 11, 2009

    AXIOM FILTERED CONNECTOR

    FDA 510(k)

    ZIMMER CONTINUUM ACETABULAR SYSTEM, ZIMMER TRILOGY IT ACETABULAR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TENOR SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC, INC.·Product code KWQ·December 11, 2009

    TAPERLOC MICROPLASTY LAT FEMORAL STEM 10.0M

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·March 6, 2013

    HYDRATOME RX SPHINCTEROTOME

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code KNS·February 15, 2011

    ATTAIN OTW

    FDA Adverse Event
    Injury ·MPRI·Product code LWP·August 8, 2014