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Results for “MONOART EM21”

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Registry EUDAMED 6 FDA 510(k) incl. De Novo FDA PMA GUDID 11

Country / market European Union (all) 6 United States 11

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Italy 6

Risk class Class I 11 Class IIa 6 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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17 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

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Registry

Class

Monoart EM21

Euronda SpA,FDA registration: Italy Group of variants

None Registry: GUDID Class:I
Monoart® Cannula EM21 EM21 Aspirator Tip EM21 Absaugkanüle

Euronda S.P.A.,Italy

Withdrawn Regimes: CE MDD, withdrawn Registry: EUDAMED Class:IIa
Monoart® EM21

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

Active Regimes: CE MDR Registry: EUDAMED Class:IIa

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