BEUDAMED
    7 results · 23ms · 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 ×

    WHITESIDE ORTHOLOC (TM)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PROTECT DROPS/SAME AS K874070

    FDA 510(k)
    FDA Class 2 ·Dental

    IMMPULSE SYSTEM

    FDA 510(k)
    FDA Class 1 ·Immunology

    TDX SALICYLATE

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    IMMULITE 2000 QUANTITATIVE CYTOMEGALOVIRUS IGG

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS·Product code LGD·June 10, 2014

    ENDOTAK ENDURANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·October 11, 2010

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code FSA·December 10, 2012