HUMASIS Covid-19 IgG/IgM Test - Indonesia BPOM Medical Device Registration
HUMASIS Covid-19 IgG/IgM Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303025287. The device is manufactured by HUMASIS CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. NEXT LEVEL MEDICAL.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HUMASIS CO., LTD.Country of Origin
Korea
Authorized Representative
PT. NEXT LEVEL MEDICALAR Address
JALAN BUKIT GADING RAYA, KOMPLEK GADING BUKIT INDAH, BLOK TB KAVLING NO. 30 LT.3
Registration Date
Jul 22, 2021
Expiry Date
Aug 02, 2025
Product Type
Serological Reagents
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