BEUDAMED
    11 results · 28ms · 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 ×

    ORCA (tm) - Operational Rescue Containment Apparatus

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814268·GENUMEDI PT SILVER R III

    BIOMET HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304007550·

    OFFSET MODULAR HEAD PROVISIONAL

    FDA UDI
    Biomet Orthopedics, LLC·00880304307988·

    LINK Instruments - Saw and drill guides

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575399581·Orthopaedic implant aiming/guiding block, reusa...

    LINK Instruments - Saw and drill guides

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575399543·Orthopaedic implant aiming/guiding block, reusa...

    HIGHLY CROSS-LINKED VITAMIN E UHMWPE TIBIAL INSERTS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MILEX CONTRACEPTIVE DIAPHRAGM, OMNIFLEX DIAPHRAGMS, ARCING DIAPHRAGMS, WIDESEAL DIAPHRAGMS

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·June 11, 2013

    ASR ACETABULAR CUPS 50

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD.·Product code KWA·July 8, 2011

    SERVO VENTILATOR 300A

    FDA Adverse Event
    Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·July 8, 2008