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Results for “REKREA”

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Registry EUDAMED 47 FDA 510(k) FDA PMA GUDID

Country / market European Union (all) 47

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Italy 47

Risk class Class I 47 Class IIa Class IIb 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) Not classified (FDA)

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47 devices foundsorted by relevance

Device · Manufacturer · Authorizations

Rekrea UDI-DI 08032909628506

Citieffe s.r.l.,Italy Class I

Active CE MDR EUDAMED I
32 variants
- Rekrea SF26010
- Rekrea SF26015
- Rekrea SF26025
- Rekrea SF26115
- Rekrea SF26150
- Rekrea SF26200
- Rekrea SF26240
- Rekrea SF26250
- Rekrea SF26305
- Rekrea SF26310
- Rekrea SF26350
- See all variants of this device
Rekrea (Small) UDI-DI 08051739538762

Citieffe s.r.l.,Italy Class I

Active CE MDR EUDAMED I
15 variants
- Rekrea (Small) SF26080
- Rekrea (Small) SF26088
- Rekrea (Small) SF26170
- Rekrea (Small) SF26172
- Rekrea (Small) SF26174
- Rekrea (Small) SF26176
- Rekrea (Small) SF26182
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Showing 21-40 of 47

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