AmoyDx® FFPE RNA Kit - Indonesia BPOM Medical Device Registration
AmoyDx® FFPE RNA Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10202320006. 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 MAIN SYNERGY PROSPEROUS.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
AMOY DIAGNOSTICS CO., LTD.Country of Origin
China
Authorized Representative
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.
Invitro Diagnostics
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AmoyDx® KRAS/NRAS Mutations Detection Kit
AmoyDx® Circulating DNA Kit
AmoyDx® Blood/Bone Marrow DNA Kit
AmoyDx® Tissue DNA Kit
AmoyDx® Tissue RNA Kit
AmoyDx® FFPE DNA/RNA Kit
AmoyDx® FFPE DNA Kit
AmoyDx® ALK Gene Fusions and ROS1 Gene Fusions Detection Kit
AmoyDx® EGFR 29 Mutations Detection Kit
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