Skip to content

Devices Categories Manufacturers Importers Certifiers Authorities Reps. Representatives

Results for “Crosstella RX”

Name, manufacturer or identifier

Manufacturer (optional)

Filters

Registry EUDAMED 144 FDA 510(k) incl. De Novo FDA PMA GUDID 192

Country / market European Union (all) 144 United States 192

More countries (1)

Belgium 144

Risk class Class I Class IIa 144 Class IIb Class III Class II (US) 48

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

192 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

Status

Regime

Registry

Class

Crosstella RX

Kaneka Corp.,Japan Group of variants

Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:IIa
R2P Crosstella RX

Kaneka Corp.,Japan Group of variants

Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:IIa
Crosstella RX

KANEKA Corporation,Japan

Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:IIa

Showing 101-120 of 192

deviCERTS Global Medical Device Regulatory Database

About [email protected]

© 2026 deviCERTS — digitaly.site