LIOFERON Tb/LTBI Human IFN- γ ELISA - Indonesia BPOM Medical Device Registration
LIOFERON Tb/LTBI Human IFN- γ ELISA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303420010. The device is manufactured by LIONEX GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FAITHFUL MEDICAL GRACE.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LIONEX GMBHCountry of Origin
Germany
Authorized Representative
PT. FAITHFUL MEDICAL GRACEAR Address
Mitra Sunter Boulevard Blok B No.39 Jl. Yos Sudarso Kav. 89
Registration Date
Jan 10, 2024
Expiry Date
May 05, 2026
Product Type
Serological Reagents
Mycobacterium tuberculosis immunofluorescent reagents.
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