BEUDAMED
    7 results · 26ms · 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.

    CORDOT R

    FDA 510(k)
    FDA Class 2 ·Microbiology

    FC-700 DEFIBRILLATOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BIO-TENS

    FDA 510(k)
    FDA Class 2 ·Neurology

    UNIFY ASSURA CRT-D, DF-4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NIK·June 6, 2014

    DEPUY ASR XL FEM IMP SIZE 49

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·December 3, 2012

    SELECT SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVN·October 5, 2010

    D & C Kit, part number CMP1466(A

    FDA Enforcement
    Class II ·Terminated·Windstone Medical Packaging, Inc.·March 8, 2017