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Results for “Morfeus”

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Registry EUDAMED 109 FDA 510(k) FDA PMA GUDID

Country / market European Union (all) 109

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Italy 100 Poland 9

Risk class Class I 109 Class IIa Class IIb Class III Class II (US)

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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109 devices foundsorted by relevance

Device · Manufacturer · Authorizations

Morfeus UDI-DI 08028540003413

MORFEUS S.p.A.,Italy Class I

Active CE MDR EUDAMED I
82 variants
- Morfeus 7011
- Morfeus 7018
- Morfeus 7022
- Morfeus 7071
- Morfeus 7112
- Morfeus 7136
- Morfeus 7159
- Morfeus 7172
- Morfeus 7178
- Morfeus 7180
- Morfeus 7184
- Morfeus 7212
- Morfeus 7231
- Morfeus N202
- See all variants of this device
Parma Reti UDI-DI 08028540008982

MORFEUS S.p.A.,Italy Class I

Active CE MDR EUDAMED I
9 variants
- Parma Reti 6712
- See all variants of this device
Febal Casa UDI-DI 08028540008234

MORFEUS S.p.A.,Italy Class I

Active CE MDR EUDAMED I
5 variants
- Febal Casa 6808
- See all variants of this device
Stilfar Italia UDI-DI 08028540009439

MORFEUS S.p.A.,Italy Class I

Active CE MDR EUDAMED I
3 variants
- See all variants of this device

Showing 61-80 of 109

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