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Results for “CytoCut”

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Registry EUDAMED 57 FDA 510(k) incl. De Novo FDA PMA GUDID 28

Country / market European Union (all) 57 United States 28

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Austria 57

Risk class Class I 14 Class IIa 57 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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71 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

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CytoCut

M.D.L. S.R.L.,Italy Group of variants

Active Regimes: CE MDD Registry: EUDAMEDGUDID Class:IIa
CytoCut

M.D.L. S.R.L.,Italy Group of variants

Active Regimes: CE MDD Registry: EUDAMED Class:IIa
CytoCut PB2110

M.D.L. S.R.L.,Italy

None Registry: GUDID Class:I
CytoCut PB2215

M.D.L. S.R.L.,Italy

None Registry: GUDID Class:I

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