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Results for “RESPIROX”

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Registry EUDAMED 9 FDA 510(k) incl. De Novo FDA PMA GUDID

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Türkiye 9

Risk class Class I Class IIa 7 Class IIb 2 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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9 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

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Respirox

Nefes Medikal Teknoloji San.tic.ltd.sti,Türkiye Group of variants

Active Regimes: CE MDR Registry: EUDAMED Class:IIa
JLO-1090Si-RespiroX

Shenzhen Homed Medical Device Co., Ltd.,China

Active Regimes: CE MDR Registry: EUDAMED Class:IIb
JLO-590i-RespiroX

Shenzhen Homed Medical Device Co., Ltd.,China

Active Regimes: CE MDR Registry: EUDAMED Class:IIb

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