BEUDAMED
    42 results · 44ms · Sources: EU EUDAMED, US FDA

    ONE-CARE OPTI Safety Lancets

    FDA registration
    MEDIVENA SP. Z O.O.·1 product·🇵🇱 Poland

    Safety Lancets Push-Button

    FDA registration
    PURCEL LABS LLC·1 product·🇺🇸 United States

    NINGBO MEDSUN MEDICAL CO., LTD.

    FDA registration
    NINGBO MEDSUN MEDICAL CO., LTD.·1 product·🇨🇳 China

    Safety Lancet

    FDA registration
    JIANGSU NEW PENTASTAR MEDICAL PRODUCTS CO. LTD.·1 product·🇨🇳 China

    SurgiLance Lite Safety Lancet

    FDA registration
    MEDIPURPOSE PTE. LTD.·1 product·🇸🇬 Singapore

    DIAGNOSTICO MEDICO SAC

    FDA registration
    DIAGNOSTICO MEDICO SAC·1 product·🇵🇪 Peru

    Safety Lancet

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

    Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

    FDA classification
    FDA Class 2 ·Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

    Brasseler USA

    FDA UDI
    Peter Brasseler Holdings, LLC·00887919678182·BR11-2220 90 X 25 MM

    Bernafon

    FDA UDI
    Bernafon AG·05714464010196·BERNAFON ALPHA 5 MNR T R MAC

    16PW - Class A 21 Lawson - Poly White

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588620909·16PW - Class A 21 Lawson - Poly White

    Samco™ Bio-Tite™ Wide Mouth, ST 90mL, 53mm, w/lab, YEL Cap

    FDA UDI
    Nalge Nunc International Corporation·10850016060713·90ML/53MM SPEC LBL OR CAP ST

    SJM Confirm Implantable Cardiac Monitor, Model DM2100

    FDA registration
    ABBOTT MEDICAL·3 products·🇺🇸 United States

    SJM Confirm Implantable Cardiac Monitor, Model DM2100

    FDA registration
    Abbott Medical·3 products·🇺🇸 United States

    Electric Scooter (FBC01, FDB05, FNS01, FNS03)

    FDA registration
    ANHUI JBH MEDICAL APPARATUS CO., LTD·1 product·🇨🇳 China

    430+

    FDA registration
    US HYPERBARIC NETWORK LLC·1 product·🇺🇸 United States

    MEDISONO, LLC

    FDA registration
    MEDISONO, LLC·3 products·🇺🇸 United States

    SJM CONFIRM IMPLANTABLE CARDIAC MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SYNTEX PRE-POWDERED NITRILE EXAMINATION GLOVE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Recorder, Event, Implantable Cardiac, (Without Arrhythmia Detection)

    FDA classification
    FDA Class 2 ·Recorder, Event, Implantable Cardiac, (Without Arrhythmia Detection)