BEUDAMED
    10,000 results · 49ms · Sources: EU EUDAMED, US FDA

    MP Biomedicals Asia Pacific Pte Ltd

    Manufacturer
    🇸🇬 Singapore·9 Basic UDI-DIs·9 Devices·bqs. s.r.o., bqs. s.r.o., bqs. s.r.o., and TÜV SÜD Product Service GmbH

    Teal Wand Vaginal Sample Self-Collection Device for Cervical Cancer Screening

    FDA registration
    DaklaPack US Inc.·1 product·🇺🇸 United States

    Teal Wand Vaginal Sample Self-Collection Device for Cervical Cancer Screening

    FDA registration
    TEAL HEALTH, INC.·1 product·🇺🇸 United States

    Kit, Dna Detection, Human Papillomavirus

    FDA Pre-Market Approval
    FDA Class 3 ·DIGENE HYBRID CAPTURE 2 (HC2) HPV DNA TEST AND DIGENE HYBRID CAPTURE 2 (HC2) HIGH-RISK HPV DNA TEST

    Kit, Dna Detection, Human Papillomavirus

    FDA Pre-Market Approval
    FDA Class 3 ·CERVISTA HPV 16/18 TEST

    Kit, Dna Detection, Human Papillomavirus

    FDA Pre-Market Approval
    FDA Class 3 ·DIGENE HYBRID CAPTURE 2 (HC2) HPV DNA TEST & HIGH RISK HPV DNA TEST

    Kit, Dna Detection, Human Papillomavirus

    FDA Pre-Market Approval
    FDA Class 3 ·CERVISTA HPV HR TEST

    Kit, Dna Detection, Human Papillomavirus

    FDA Pre-Market Approval
    FDA Class 3 ·BD ONCLARITY HPV ASSAY

    MAVEN PRO

    FDA 510(k)
    FDA Class 2 ·Radiology

    LIPIFLOW THERMAL PULSATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    SOFTLIGHT Q-SWITCHED ND: YAG LASER WITH OPTIONAL BEAM-SHRINKING HANDPIECE ACCESSORY

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

    BrachyGel Vaginal Hydrogel Packing System

    FDA 510(k)
    FDA Class 2 ·Radiology

    GH DISPOSABLE AND GH REUSABLE BLOOD PRESSURE CUFF

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    KOSTEC MEDICAL GRADE LDC MONITORS

    FDA 510(k)
    FDA Class 2 ·Radiology

    Kit, Dna Detection, Human Papillomavirus

    FDA Pre-Market Approval
    FDA Class 3 ·CERVISTA HPV HR COMPONENTS

    K-Z iTURN

    FDA UDI
    KAP MEDICAL·00817012030167·Alternating Rotation, Auto Immersion, Pulsation...

    Kit, Dna Detection, Human Papillomavirus

    FDA Pre-Market Approval
    FDA Class 3 ·CERVISTA HPV 16/18

    SOLOPAK BRAND FILTER NEEDLE W/5 MICRO

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MAX-I-PROBE PERIODONTAL ENDODONTIC PROB

    FDA 510(k)
    FDA Class 1 ·Dental

    MICRO Z DISPOS. SPINAL ANESTH. NEEDLE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology