MAGPIX - Indonesia BPOM Medical Device Registration
MAGPIX is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20102917535. 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
Oct 28, 2021
Expiry Date
May 21, 2025
Product Type
Clinical Laboratory Equipment
Instrumentation for clinical multiplex test systems.
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