BEUDAMED
    18 results · 7ms · Sources: EU EUDAMED, US FDA

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    Filters Classification: FDA Class 2 × Regulation: Us FDA × Clear all

    CARL ZEISS INN MYRINGOTOMY TUBE LINE

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    ANNE Pediatric

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ANNE One

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ANNE Sleep

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ANNE Maternal

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ANNE Limb

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ANNE One

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ANNE Chest

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PROVIDER ANNE INFUSER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ANNE View, Central Hub

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CAS 740 SERIES MONITOR, MODELS 740-1, 740M-1, 740-2MS, 740M-2MS, 740-2NL, 740M-2NL, 740-2NN, 740M-2NN, 740-3MS, 740M-3MS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Tetrazolium Int Dye-Diaphorase, Lactate Dehydrogenase

    FDA classification
    FDA Class 2 ·Tetrazolium Int Dye-Diaphorase, Lactate Dehydrogenase

    Monitor, Uterine Contraction, External (For Use In Clinic)

    FDA Pre-Market Approval
    FDA Class 2 ·GENESIS SYSTEM & TERM GUARD I & TERM GUARD II SYS.

    Monitor, Uterine Contraction, External (For Use In Clinic)

    FDA Pre-Market Approval
    FDA Class 2 ·GENESIS SYSTEM & TERM GUARD I & TERM GUARD II SYS.

    Monitor, Uterine Contraction, External (For Use In Clinic)

    FDA Pre-Market Approval
    FDA Class 2 ·GENESIS HOME UTERINE ACTIVITY MONITORING SYSTEM (HUAM)

    Monitor, Uterine Contraction, External (For Use In Clinic)

    FDA Pre-Market Approval
    FDA Class 2 ·GENESIS(R) HOME UTERINE ACTIVITY MONITORING SYSTEM

    Calibrators, Ethyl Alcohol

    FDA classification
    FDA Class 2 ·Calibrators, Ethyl Alcohol

    Device For Home Collection And Transport Of Vaginal Specimens By Lay Users For Use In An Approved Hpv Molecular Assay

    FDA classification
    FDA Class 2 ·Device For Home Collection And Transport Of Vaginal Specimens By Lay Users For Use In An Approved Hpv Molecular Assay