ARIES® HSV 1&2 Assay - Indonesia BPOM Medical Device Registration
ARIES® HSV 1&2 Assay is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303025620. The device is manufactured by LUMINEX CORPORATION from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is GENECRAFT LABS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LUMINEX CORPORATIONCountry of Origin
United States
Authorized Representative
GENECRAFT LABSAR Address
Business Park kebon Jeruk Blok F2 No 9 Jl. Meruya Ilir Raya No. 88
Registration Date
Sep 25, 2020
Expiry Date
Jun 18, 2025
Product Type
Serological Reagents
Herpes simplex virus serological assays.
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