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Results for “NEVIO”

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Registry EUDAMED 41 FDA 510(k) FDA PMA GUDID 1

Country / market European Union (all) 41 United States 1

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Italy 41

Risk class Class I 42 Class IIa Class IIb Class III Class II (US)

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)

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42 devices foundsorted by relevance

Device · Manufacturer · Authorizations

Serena UDI-DI 08051881022195

Chinesport S.P.A.,Italy Class I

Active CE MDR EUDAMED I
26 variants
- Serena LZ212A1W3
- Serena LZ212D1W1
- Serena LZ212D2W2
- Serena LZ212D2W3
- Serena LZ212D2WE
- Serena LZ212D2WN
- Serena LZ212D2WT
- Serena LZ212D2X3
- Serena LZ213C1W8
- Serena LZ213C2W3
- Serena LZ213D1W3
- Serena LZ213D2W3
- See all variants of this device
Nevio UDI-DI 08051881011212

Chinesport S.P.A.,Italy Class I

Active CE MDR EUDAMED I
14 variants
- Nevio LZ112C1W3
- Nevio LZ112D1W3
- Nevio LZ112D1WR
- Nevio LZ112D2W7
- Nevio LZ112D2WL
- Nevio LZ112D2XR
- See all variants of this device

Showing 21-40 of 42

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