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Results for “PFT 2820”

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Registry EUDAMED FDA 510(k) FDA PMA GUDID 38

Country / market United States 38

Risk class Class I Class IIa Class IIb Class III Class II (US) 38

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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38 devices foundsorted by relevance

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Pft 2820 UDI-DI 05099169284432

Vitalograph Ireland, Ltd.,Ireland(FDA 510(k) applicant) Class II

None GUDID II
38 variants
- Pft 2820 2820 UDI-DI 05099169283701
- Pft 2820 2820 UDI-DI 05099169283725
- Pft 2820 2820 UDI-DI 05099169283855
- Pft 2820 2820 UDI-DI 05099169284029
- Pft 2820 2820 UDI-DI 05099169284180
- Pft 2820 2820 UDI-DI 05099169284258
- Pft 2820 2820 UDI-DI 05099169284302
- Pft 2820 2820 UDI-DI 05099169284326
- Pft 2820 2820 UDI-DI 05099169284371
- Pft 2820 2820 UDI-DI 05099169284401
- Pft 2820 2820 UDI-DI 05099169284487
- Pft 2820 2820 UDI-DI 05099169285514
- Pft 2820 2820 UDI-DI 05099169285521
- Pft 2820 2820 UDI-DI 55099169283713
- Pft 2820 2820 UDI-DI 55099169283812 Withdrawn
- Pft 2820 2820 UDI-DI 55099169284277
- See all variants of this device

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