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Registry EUDAMED FDA 510(k) incl. De Novo 43 FDA PMA GUDID

Country / market United States 43

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

More classes (11)

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: Imed Corp.× Clear all

DeviceDevice · Manufacturer · Authorizations Verified

Status

Regime

Registry

Class

Shrouded Needle Devices

Imed Corp.,United States(FDA applicant)

Active Regimes: 510(k) Registry: 510(k) Class:II
Imed 4100 And 4200 Disposable Infusion Devices Mod

Imed Corp.,United States(FDA applicant)

Active Regimes: 510(k) Registry: 510(k) Class:II
Accuset Administration Set

Imed Corp.,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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