BEUDAMED
    12 results · 19ms · Sources: EU EUDAMED, US FDA

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    K-ASSAY RHEUMATOID FACTOR

    FDA 510(k)
    FDA Class 2 ·Immunology

    GentleYAG

    FDA UDI
    Candela Corporation·00817495020129·Pulsed Laser Previous DI: 08174950200123

    GentleYAG LE

    FDA UDI
    Candela Corporation·00817495022659·Pulsed Laser

    GentleYAG LE

    FDA UDI
    Candela Corporation·00817495022642·Pulsed Laser

    GentleYAG

    FDA UDI
    Candela Corporation·00817495021119·Pulsed Laser

    GentleYAG

    FDA UDI
    Candela Corporation·00817495021126·Pulsed Laser

    PRECEPT MICRO-GARD LASER MASK

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    LIGHTCYCLER MRSA ADVANCED TEST FOR USE WITH THE LIGHTCYCLER 2.0 INSTRUMENT, MODEL 05205727

    FDA 510(k)
    FDA Class 2 ·Microbiology

    GO BED PLUS

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·March 6, 2013

    ATTAIN OTW

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014

    LIGHTCYCLER MRSA ADVANCED TEST FOR USE WITH THE LIGHTCYCLER 2.0 INSTRUMENT

    FDA Adverse Event
    ROCHE MOLECULAR SYSTEMS·Product code OOI·July 11, 2012