MAGLUMI Toxo IgG (CLIA) - Indonesia BPOM Medical Device Registration
MAGLUMI Toxo IgG (CLIA) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303816144. The device is manufactured by SHENZHEN NEW INDUSTRIES BIOMEDICAL ENGINEERING CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MULTIMEDILAB KARYAMANDIRI.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
China
Authorized Representative
PT. MULTIMEDILAB KARYAMANDIRIAR Address
GP plaza lantai 3 unit 6, jalan Gelora II No. 01
Registration Date
Jan 24, 2023
Expiry Date
Dec 31, 2025
Product Type
Serological Reagents
Toxoplasma gondii serological reagents.
Invitro Diagnostics
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MAGLUMI 4000 CLIA Analyzer and Accessories
Maglumi™ Light Check
MAGLUMI 800 CLIA Analyzer and Accessories
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