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Results for “MONOART EM19”

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Registry EUDAMED 8 FDA 510(k) incl. De Novo FDA PMA GUDID 8

Country / market European Union (all) 8 United States 8

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Italy 8

Risk class Class I 8 Class IIa 8 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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16 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

Status

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Registry

Class

Monoart EM19

Euronda SpA,FDA registration: Italy Group of variants

None Registry: GUDID Class:I
Monoart® EM19

Euronda S.P.A.,Italy Group of variants

Active Regimes: CE MDR Registry: EUDAMED Class:IIa
Monoart® Cannula EM19 EM19 Aspirator Tip EM19 Absaugkanüle

Euronda S.P.A.,Italy

Withdrawn Regimes: CE MDD, withdrawn Registry: EUDAMED Class:IIa

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