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Results for “Eonis”

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Registry EUDAMED 48 FDA 510(k) 3 FDA PMA GUDID 45

Country / market European Union (all) 47 United States 48

More countries (2)

Belgium 41 Finland 6

Risk class Class I 43 Class IIa Class IIb Class III Class II (US) 5

More classes (11)

Class A 3 Class B Class C 1 Class D IVD General 2 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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54 devices foundsorted by relevance

Device · Manufacturer · Authorizations

Eonis UDI-DI 05415334045736

Barco NV,Belgium Class I

Active CE MDR EUDAMEDGUDID I
38 variants
- Eonis K9301820A
- Eonis K9307935B
- Eonis K9307942
- Eonis K9307942B
- Eonis K9307944BR Withdrawn
- Eonis K9307945
- Eonis K9307947B
- Eonis K9307953
- Eonis K9350030
- Eonis K9356021A1X
- Eonis K9356033A1X
- Eonis K9356034A1X
- Eonis K9356035A1X
- Eonis K9356036A1X
- Eonis K9356038A1X
- Eonis K9356040A1X
- See all variants of this device
Eonis 32”

Barco NV,Belgium Class I

Active CE MDR EUDAMEDGUDID I

Showing 21-40 of 54

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