BEUDAMED
    8 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 ×

    MISHLER 2 CHAMB FLUSHING VALVE,STAND

    FDA 510(k)
    FDA Class 2 ·Neurology

    CAM Titanium Blanks

    FDA 510(k)
    FDA Class 2 ·Dental

    SYNTHETIC VINYL PATIENT EXAMINATION GLOVE-POWERED

    FDA 510(k)
    FDA Class 1 ·General Hospital

    COBAS 8000 C 702 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·April 8, 2024

    HEARTMATE II LVAS, EUROPE

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·April 7, 2014

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·September 26, 2012

    ALLERGAN

    FDA Adverse Event
    Malfunction ·ALLERGAN, INC.·Product code FWM·July 13, 2010

    Model Number U228, VISIONIST CRT-P EL MRI

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025