BEUDAMED
    6 results · 17ms · 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.

    SINGLE PATIENT SYS. II MODEL DM-450

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    RAMPART-O, RAMPART-T

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SimpleSense-BP, SimpleSense-BP Software Application

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ARIS TRANS-OBUTRATOR

    FDA Adverse Event
    Injury ·COLOPLAST A/S·Product code FTL·February 7, 2014

    DIRECT DRIVE DISPOSABLE CLIP APPLIER 10MM 3/BOX

    FDA Adverse Event
    APPLIED MEDICAL·Product code FZP·October 26, 2012

    IAB:8 FR - 40 CC

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DSP·September 3, 2010