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Registry EUDAMED FDA 510(k) 34 FDA PMA GUDID 324

Country / market United States 358

Risk class Class I 20 Class IIa Class IIb Class III Class II (US) 338

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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358 devices foundsorted by relevance

Manufacturer: Vitalograph, Ltd.× Clear all

Device · Manufacturer · Authorizations

Model 4000 UDI-DI 05099169402669

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

None GUDID II
111 variants
- Model 4000 4000 UDI-DI 05099169400320 Withdrawn
- Model 4000 4000 UDI-DI 05099169402744
- Model 4000 4000 UDI-DI 05099169404038
- Model 4000 4000 UDI-DI 05099169404496
- Model 4000 4000 UDI-DI 05099169407008
- Model 4000 4000 UDI-DI 05099169407503
- Model 4000 4000 UDI-DI 35099169402493
- Model 4000 4000 UDI-DI 35099169403636 Withdrawn
- Model 4000 4000 UDI-DI 35099169405500
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Pft 2820 UDI-DI 05099169284302

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

None GUDID II
38 variants
- Pft 2820 2820 UDI-DI 05099169283855
- Pft 2820 2820 UDI-DI 05099169284487
- Pft 2820 2820 UDI-DI 05099169285521
- Pft 2820 2820 UDI-DI 55099169283812 Withdrawn
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Alpha 6000 UDI-DI 05099169650183

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

None GUDID II
47 variants
- Alpha 6000 6000
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Bvf 2820 UDI-DI 05099169283831

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

None GUDID II
28 variants
- Bvf 2820 2820
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Pneumotrac 6800 UDI-DI 05099169770010

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

None GUDID II
12 variants
- See all variants of this device

Showing 101-120 of 358

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