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Results for “Neen”

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Registry EUDAMED 3 FDA 510(k) incl. De Novo 1 FDA PMA GUDID

Country / market European Union (all) 3 United States 1

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4 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

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Periform Perineometric Probe, Model 8300

Neen Design, Ltd.,United Kingdom(FDA applicant)

Active Regimes: 510(k) Registry: 510(k) Class:II
Neenca

Shenzhen Haofan Network Technology Co., LTD.,China

Active Regimes: CE MDR Registry: EUDAMED Class:I
Neen

Performance Health International LTD,United Kingdom Group of variants

Active Regimes: CE MDD Registry: EUDAMED Class:IIa

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