ARIES® System - Indonesia BPOM Medical Device Registration
ARIES® System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304024273. 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 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
Aug 04, 2020
Expiry Date
May 21, 2025
Product Type
Immunology Laboratory Equipment and Reagents
RNA Preanalytical Systems.
Invitro Diagnostics
LABScan 3D Verification Kit
LABScan 3D Calibration Kit
FLEXMAP 3D® System
FLEXMAP 3D Performance Verification Kit
FLEXMAP 3D Calibration Kit
ARIES SARS-CoV-2 Assay Kit
ARIES® Flu A/B & RSV Assay
MAGPIX
MAGPIX Calibration Kit
MAGPIX Performance Verification Kit
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