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Results for “BEIWO”

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Registry EUDAMED 8 FDA 510(k) incl. De Novo FDA PMA GUDID

Country / market European Union (all) 8

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Austria 6 Spain 1 Ireland 1

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

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Class A 8 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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8 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

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Pathogen DNA/RNA Purification Kit (Beads)

Hangzhou Beiwo Medical Technology Co., Ltd.,China

Active Regimes: CE IVDR Registry: EUDAMED Class:A
Beiwo

Hangzhou Beiwo Medical Technology Co., Ltd.,China Group of variants

Active Regimes: CE IVDR Registry: EUDAMED Class:A
no

Hangzhou Beiwo Medical Technology Co., Ltd.,China

Active Regimes: CE IVDR Registry: EUDAMED Class:A

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