AmoyDx® FFPE DNA Kit - Indonesia BPOM Medical Device Registration
AmoyDx® FFPE DNA Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10202320007. The device is manufactured by AMOY DIAGNOSTICS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MAIN SYNERGY PROSPEROUS.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
AMOY DIAGNOSTICS CO., LTD.Country of Origin
China
Authorized Representative
PT. MAIN SYNERGY PROSPEROUSAR Address
Gedung Menara Salemba Lt.3, Jl. Salemba Raya No.5-5A
Registration Date
Jun 21, 2023
Expiry Date
Dec 15, 2027
Product Type
Cell and Tissue Culture Products
Cell and tissue culture supplies and equipment.
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