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Registry EUDAMED 156 FDA 510(k) FDA PMA GUDID

Country / market European Union (all) 156

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Italy 114 France 42

Risk class Class I 156 Class IIa Class IIb Class III Class II (US)

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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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156 devices foundsorted by relevance

Manufacturer: Sanyleg SRL× Clear all

Device · Manufacturer · Authorizations

Mediven 20 Biosoft Bas Jarret UDI-DI 08057628870685

Sanyleg SRL,Italy Class I

Active CE MDR EUDAMED I
42 variants
- Mediven 20 Biosoft Bas Jarret F104128000
- Mediven 20 Biosoft Bas Jarret F104144000
- Mediven 20 Biosoft Bas Jarret F104147000
- Mediven 20 Biosoft Bas Jarret F104155000
- Mediven 20 Biosoft Bas Jarret F104158000
- Mediven 20 Biosoft Bas Jarret F104159000
- Mediven 20 Biosoft Bas Jarret F104161000
- Mediven 20 Biosoft Bas Jarret F104162000
- Mediven 20 Biosoft Bas Jarret F104166000
- See all variants of this device
Sanyleg Knee-High UDI-DI 08033201402672

Sanyleg SRL,Italy Class I

Active CE MDR EUDAMED I
110 variants
- Sanyleg Knee-High B12 UDI-DI 08033201402405
- Sanyleg Knee-High B12 UDI-DI 08033201402504
- Sanyleg Knee-High B12 UDI-DI 08052204151783
- Sanyleg Knee-High B12 UDI-DI 08052204151813
- Sanyleg Knee-High C02 UDI-DI 08033201402191
- Sanyleg Knee-High C02 UDI-DI 08033201402221
- Sanyleg Knee-High C02 UDI-DI 08033201402320
- Sanyleg Knee-High C02 UDI-DI 08033201402344
- Sanyleg Knee-High P22
- See all variants of this device

Showing 81-100 of 156

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