ARIES SARS-CoV-2 Assay Kit - Indonesia BPOM Medical Device Registration
ARIES SARS-CoV-2 Assay Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303127167. The device is manufactured by LUMINEX CORPORATION from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GENECRAFT LABS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LUMINEX CORPORATIONCountry of Origin
United States
Authorized Representative
PT. GENECRAFT LABSAR Address
Business Park kebon Jeruk Blok F2 No 9 Jl. Meruya Ilir Raya No. 88
Registration Date
Nov 16, 2022
Expiry Date
Jun 02, 2026
Product Type
Serological Reagents
Respiratory viral panel multiplex nucleic acid assay
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