BEUDAMED
    30 results · 21ms · 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 ×

    STAYHEALTHY BODY COMPOSITION MONITOR-BCM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814589·GENUMEDI SAND SIZE VII

    ILIZAROV SYSTEMS

    FDA UDI
    MEDICALPLASTIC SRL·08033201841655·SHORT CONNECTION PLATE 115MM

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964068669·The ENDO CARRY-ON Procedure Kit contains all of...

    TRILOGY

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·February 12, 2025

    LEKON

    FDA UDI
    C A I INDUSTRIES CORP·00807689004356·acupuncture needles

    Complete Cervical

    FDA UDI
    Seaspine Orthopedics Corporation·10889981040505·Implant - 18x15x7mm - 6 deg

    Vasomedical-Biox™ Model 1807 Ambulatory Blood Pressure Recorder w/Bluetooth

    FDA UDI
    VASOMEDICAL, INC.·00817980020481·Model 1807 Ambulatory Blood Pressure Recorder w...

    Vasomedical-Biox™ 1807 ABP Monitor With Analysis S/W w/ Bluetooth

    FDA UDI
    VASOMEDICAL, INC.·00817980020061·Ambulatory Blood Pressure Recorder w/Bluetooth

    TISSUE MARKER

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    SCS CLARIS SPINAL SCREWS, TYPES V,G,E

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    KENDALL

    FDA Adverse Event
    Malfunction ·KENDALL·Product code FMF·August 16, 2011

    Ascendant

    FDA UDI
    Choice Spine, LP·10885862260642·

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code NKB·May 1, 2014

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·October 2, 2012

    CABLE TENSIONER

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code KTT·December 11, 2012

    MAGNUM DISPOSABLE CORE BIOPSY NEEDLE

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code FCG·May 1, 2013

    SHILEY DISPOSABLE CANNULA LPC

    FDA Adverse Event
    Injury ·COVIDIEN/FORMERLY TYCO HEALTHCARE·Product code BTO·August 6, 2008

    6600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 10, 2011

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code NKB·May 25, 2016