BEUDAMED
    9 results · 29ms · 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 ×

    CONTACT EMG ROTATABLE ENDOTRACHEAL TUBE

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    SOLIDEA

    FDA UDI
    CALZIFICIO PINELLI SRL·08300496050162·RED WELLNESS 70 LEGGINGS, SIZE XL, NERO, GRADUA...

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450483862·

    EQUINOX OCCULSION BALLOON SYSTEM MODEL # 104-4015, 104-4018, 104-4021, 104-4023, 104-4026

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    METRISCAN BONE DENSITY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·April 10, 2013

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·April 1, 2011

    ST. JUDE

    FDA Adverse Event
    Injury ·ST. JUDE·Product code DTB·May 14, 2008

    Belmont Rapid Infuser, a Fluid Management System, Model FMS2000.

    FDA Enforcement
    Class II ·Terminated·Belmont Instrument Corporation·October 24, 2012