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Results for “Arietta 65”

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Registry EUDAMED 2 FDA 510(k) incl. De Novo 2 FDA PMA GUDID 3

Country / market United States 5

Risk class Class I Class IIa Class IIb Class III Class II (US) 5

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Class A Class B Class C Class D IVD General IVD Annex II List A IVD Annex II List B IVD for self-testing Active implantable (AIMDD) Unclassified (FDA) Not classified (FDA)

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5 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

Status

Regime

Registry

Class

Arietta 65

Fujifilm Corporation,Japan

Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
Arietta 650

Fujifilm Corporation,Japan

Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
Hitachi Arietta 65

Hitachi, Ltd.,Japan

Withdrawn Registry: GUDID Class:II
Arietta 65 Open recall

Hitachi Healthcare Americas Corporation,United States(FDA applicant) Group of variants

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

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