BEUDAMED
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    EPTE SYSTEM

    Device
    EU MDR · Eu Md Class 2a ·IONCLINICS & DEIONIC, S.L.·On the market·1 country

    EPTE BIPOLAR tDCS

    Device
    EU MDR · Eu Md Class 2a ·IONCLINICS & DEIONIC, S.L.·On the market·1 country

    EPTE BIPOLAR System

    Device
    EU MDR · Eu Md Class 2a ·IONCLINICS & DEIONIC, S.L.·On the market·1 country

    e.p.t. Digital Early Pregnancy Test

    FDA UDI
    Prestige Consumer Healthcare Inc.·00363736993030·e.p.t.® Digital 3 Ct

    e.p.t. Direct

    FDA UDI
    Nfi Consumer Products·00045611963030·e.p.t. Direct 3 ct.

    e.p.t. Direct

    FDA UDI
    Nfi Consumer Products·00045611962026·e.p.t. Direct 2 ct.

    e.p.t. Analog

    FDA UDI
    Nfi Consumer Products·00045611952027·e.p.t. Analog 2 Ct

    e.p.t. Early Pregnancy Test

    FDA UDI
    Prestige Consumer Healthcare Inc.·00363736952020·e.p.t.® Analog 2 Ct

    e.p.t. Digital Early Pregnancy Test

    FDA UDI
    Prestige Consumer Healthcare Inc.·00363736992026·e.p.t.® Digital 2 Ct

    e.p.t. Early Pregnancy test

    FDA UDI
    Prestige Consumer Healthcare Inc.·00363736953034·e.p.t.® Analog 3 Ct

    N/A

    FDA UDI
    STRYKER SUSTAINABILITY SOLUTIONS, INC.·00885825008475·Diagnostic EP Catheter Cournand Curve, electrod...

    N/A

    FDA UDI
    STRYKER SUSTAINABILITY SOLUTIONS, INC.·00885825007898·Steerable Diagnostic EP Catheter , STANDARD, 4 ...

    EPT CERTAINTY PREGNANCY TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    EPT Menopause (FSH) Rapid Test

    FDA UDI
    Hangzhou AllTest Biotech Co., Ltd.·20045611954018·

    ENTERIC PATHOGEN TRANSPORT (EPT) (E1020,E1000)

    FDA 510(k)
    FDA Class 1 ·Microbiology

    NA

    FDA UDI
    GE Healthcare Finland Oy·00840682104128·

    Cable, Return for RF/Bovie (EPT) (~10ft)

    FDA UDI
    Tz Medical, Inc.·00811331017434·Cable, Return for RF/Bovie (EPT) (~10ft)

    EPT-1000 TC AUTOMATIC PERSONALITY MODULE (APM)

    FDA Adverse Event
    Malfunction ·EPT/A DIVISION OF BSC·Product code GXD·October 6, 2000

    EPT-1000XP? RF ABLATION SYSTEM - FOOT SWITCH

    FDA Adverse Event
    Malfunction ·PLEXUS SERVICES CORPORATION·Product code OAD·June 20, 2013

    BLAZER II HTD

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CARDIOVASCULAR DIVISION·Product code LPB·July 13, 2009