BEUDAMED
    9 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 ×

    NAUTILUS SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Freedom Pedicle Screw System

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215027490·

    AXOGUARD NERVE CONNECTOR AND PROTECTOR

    FDA Adverse Event
    Injury ·COOK BIOTECH·Product code JXI·August 24, 2015

    APAX PACS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    ATLAS HOME PREGNANCY TEST (MIDSTREAM FORMAT) MODEL 70172001

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 29, 2013

    COMPOSITCP 30 INTERFERENCE SCREW

    FDA Adverse Event
    Malfunction ·BIOMET SPORTS MEDICINE·Product code HWC·June 17, 2011

    RUNWAY GUIDE CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQY·August 22, 2008

    AXOGUARD NERVE CONNECTOR AND PROTECTOR

    FDA Adverse Event
    Injury ·COOK BIOTECH·Product code JXI·October 24, 2019