BEUDAMED
    9 results · 22ms · 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 ×

    VARICELLA-ZOSTER(IGG) IFA TEST

    FDA 510(k)
    FDA Class 2 ·Microbiology

    SOLE MEDIAL COLUMN FUSION PLATE

    FDA UDI
    ORTHOFIX SRL·18053340348102·SS VA LOCKING SCREW L34MM D4MM

    SOLE MEDIAL COLUMN FUSION PLATE

    FDA UDI
    ORTHOFIX SRL·18053340346962·SS VA LOCKING SCREW L34MM D4MM STERILE

    SATURN 5 LASER

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

    C3 AND LIFEGARD ICG IMPEDANCE CARDIOGRAPHY MONITORS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·May 30, 2014

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 23, 2012

    SINGLE USE RESUSCITATION CIRCUIT KIT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE, LTD.·Product code BTL·September 15, 2010

    ENDOPLEGE CORONARY SINUS CATHETER

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES·Product code DWF·June 16, 2011