BEUDAMED
    11 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 ×

    Fully Automatic Electronic Blood Pressure Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Vanguard® Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00880304271524·

    Percutaneous Compression Plate (PC.C.P)

    FDA UDI
    ORTHOFIX SRL·18032568866100·GOTFRIED PC.C.P. SHAFT SCREW - 34 MM "PACK OF 5"

    Percutaneous Compression Plate (PC.C.P)

    FDA UDI
    ORTHOFIX SRL·18033509850660·GOTFRIED PC.C.P. SHAFT SCREW - 34 MM "PACK OF 5...

    GLIDERXTREME PTA BALLOON CATHETER (CB) (OVER THE WIRE) 0.014 / 0.018 GUIDE WIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LIFEBED NETWORK PATIENT VIGILANCE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 18, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 22, 2013

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·July 11, 2011

    REVERSE SHOULDER SYSTEM GLENOSPHERE 39X27

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·May 8, 2020

    REVERSE SHOULDER SYSTEM 04.01.0172 GLENOSPHERE 36XØ27

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·December 6, 2023