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.

    ROTALEX 2 LATEX AGGLUTINATION TEST FOR ROTAVIRUS

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Spectrum-2

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MEDELA APGAR TIMER

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ACCU-CHEK ® MOBILE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·June 6, 2014

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·December 3, 2012

    RESTORE ULTRA

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·September 30, 2010