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Results for “Activon Tulle”

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Registry EUDAMED 2 FDA 510(k) incl. De Novo 1 FDA PMA GUDID 2

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Ireland 2

Risk class Class I Class IIa Class IIb 2 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) 1 Not classified (FDA)

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5 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

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Registry

Class

Activon Tulle CR4135

Brightwake Limited,United Kingdom

None Registry: GUDID Class:—
Activon Tulle CR4136

Brightwake Limited,United Kingdom

Active Regimes: CE MDD Registry: GUDID Class:—
Activon Tulle

Calidad Solutions, Inc.,FDA registration: United States

Active Regimes: 510(k) Registry: 510(k) Class:—
Activon Tulle

Brightwake Limited,United Kingdom Group of variants

Active Regimes: CE MDD Registry: EUDAMED Class:IIb

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