VivaDiag™ Progesterone Test Kit (FIA) - Indonesia BPOM Medical Device Registration
VivaDiag™ Progesterone Test Kit (FIA) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101520191. The device is manufactured by VIVACHEK BIOTECH (HANGZHOU) CO., LTD., CHINA. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MAIN MEDICAL CHAKRA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
VIVACHEK BIOTECH (HANGZHOU) CO., LTD., CHINA.Country of Origin
China
Authorized Representative
PT. MAIN MEDICAL CHAKRAAR Address
FORESTA BUSINESS LOFT 6 No. 10, Jl. Raya Boulevard Utara BSD City, Desa/Kelurahan Lengkong Kulon
Registration Date
Jan 24, 2025
Expiry Date
Nov 23, 2028
Product Type
Clinical Chemistry Test System
Progesterone test system (card)
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