BEUDAMED
    8 results · 19ms · 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 ×

    Hydroven 12, Hydroven 12 Garments

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VITEK 2 STREPTOCOCCUS LEVOFLOXACIN

    FDA 510(k)
    FDA Class 2 ·Microbiology

    SMIT SLEEVE

    FDA 510(k)
    FDA Class 2 ·Radiology

    ATTAIN OTW

    FDA Adverse Event
    Injury ·MPRI·Product code LWP·June 7, 2013

    6800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 23, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 10, 2008

    AMS 800 URINARY CONTROL SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code EZY·October 15, 2018

    PUMP 1886 780G OUS BLE PUMP MG/DL

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·March 31, 2026