Skip to content

Devices Categories Manufacturers Importers Certifiers Authorities Reps. Representatives

Results for “ALOKA ARIETTA 850”

Name, manufacturer or identifier

Manufacturer (optional)

Filters

Registry EUDAMED 1 FDA 510(k) incl. De Novo 3 FDA PMA GUDID 2

Country / market United States 5

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

More classes (11)

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)

Verified Verified only

Category (EMDN)

Browse by category

5 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

Status

Regime

Registry

Class

Aloka Arietta 850

Fujifilm Corporation,Japan

Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
HITACHI Aloka Arietta 850

Hitachi, Ltd.,Japan

Withdrawn Registry: GUDID Class:II
Aloka Arietta 850 Open recall

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

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

Previous Next

Showing 1-5 of 5

deviCERTS Global Medical Device Regulatory Database

About [email protected]

© 2026 deviCERTS — digitaly.site