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Results for “BIOSORB OTIS 50”

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Registry EUDAMED 7 FDA 510(k) FDA PMA GUDID 10

Country / market United States 10

Risk class Class I Class IIa Class IIb Class III Class II (US) 10

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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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10 devices foundsorted by relevance

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Biosorb Otis 50 UDI-DI 03760154002073

S.B.M,FDA registration: United States

Active Regimes: CE MDD Registry: EUDAMEDGUDID Class:II
7 variants
- Biosorb Otis 50 P822367222
- Biosorb Otis 50 P822367224
- Biosorb Otis 50 P822367228
- Biosorb Otis 50 P822367230
- Biosorb Otis 50 P822367232
- Biosorb Otis 50 P822367234
Biosorb Otis 50 UDI-DI 03760154002141

S.B.M,FDA registration: United States

Withdrawn Registry: GUDID Class:II
3 variants
- Biosorb Otis 50 P822367236 Withdrawn
- Biosorb Otis 50 P822367238 Withdrawn

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