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Registry EUDAMED FDA 510(k) 43 FDA PMA GUDID

Country / market United States 43

Risk class Class I 1 Class IIa Class IIb Class III Class II (US) 42

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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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43 devices foundsorted by relevance

Manufacturer: Erika, Inc.× Clear all

DeviceDevice · Manufacturer · Authorizations Verified

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Erika Heparin Infusion Adaptor

Erika, Inc.,United States(FDA applicant)

Active Regimes: 510(k) Registry: 510(k) Class:II
Erika Negative Pressure Venous Bl Sets

Erika, Inc.,United States(FDA applicant)

Active Regimes: 510(k) Registry: 510(k) Class:II
Modification To Kidney Dialyzer

Erika, Inc.,United States(FDA applicant)

Active Regimes: 510(k) Registry: 510(k) Class:II

Showing 41-43 of 43

deviCERTS Global Medical Device Regulatory Database

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