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Registry EUDAMED FDA 510(k) incl. De Novo 22 FDA PMA GUDID

Country / market United States 22

Risk class Class I Class IIa Class IIb Class III Class II (US) 22

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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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22 devices foundsorted by relevance

Manufacturer: Philips Medizinsysteme Boeblingen GmbH, Cardiac AN× Clear all

DeviceDevice · Manufacturer · Authorizations Verified

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MP5 Intellivue Patient Monitor

Philips Medizinsysteme Boeblingen GmbH, Cardiac AN,Germany(FDA applicant)

Active Regimes: 510(k) Registry: 510(k) Class:II
Philips Intellivue TCG10

Philips Medizinsysteme Boeblingen GmbH, Cardiac AN,Germany(FDA applicant)

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

Showing 21-22 of 22

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