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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

Sanyleg Knee-High UDI-DI 08033201402511

Sanyleg SRL,Italy Class I

Active CE MDR EUDAMED I
110 variants
- Sanyleg Knee-High B12 UDI-DI 08033201402535
- Sanyleg Knee-High B12 UDI-DI 08033201402542
- Sanyleg Knee-High B12 UDI-DI 08033201402573
- Sanyleg Knee-High B12 UDI-DI 08052204151745
- Sanyleg Knee-High C02 UDI-DI 08033201402276
- Sanyleg Knee-High C02 UDI-DI 08033201402351
- Sanyleg Knee-High C02 UDI-DI 08052204151387
- Sanyleg Knee-High M32 UDI-DI 08033201402887
- Sanyleg Knee-High M32 UDI-DI 08033201402979
- Sanyleg Knee-High P22 UDI-DI 08033201402627
- Sanyleg Knee-High P22 UDI-DI 08033201402634
- Sanyleg Knee-High P22 UDI-DI 08033201402696
- Sanyleg Knee-High P22 UDI-DI 08033201402757
- Sanyleg Knee-High P22 UDI-DI 08033201405840
- See all variants of this device
Mediven 20 Biosoft Bas Jarret UDI-DI 08057628870616

Sanyleg SRL,Italy Class I

Active CE MDR EUDAMED I
42 variants
- Mediven 20 Biosoft Bas Jarret F104139000
- Mediven 20 Biosoft Bas Jarret F104143000
- Mediven 20 Biosoft Bas Jarret F104154000
- Mediven 20 Biosoft Bas Jarret F104157000
- See all variants of this device

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