RapidLight Total T3 CLIA Test - Indonesia BPOM Medical Device Registration
RapidLight Total T3 CLIA Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101322968. The device is manufactured by CTK BIOTECH, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. RAJAERBA INDOCHEM.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CTK BIOTECH, INC.Country of Origin
United States
Authorized Representative
PT. RAJAERBA INDOCHEMAR Address
Jl. Hj. Tutty Alawiyah No. 8, Desa/Kelurahan Duren Tiga, Kec. Pancoran, Kota Adm. Jakarta Selatan, Provinsi DKI Jakarta, Kode Pos: 12760
Registration Date
Apr 20, 2023
Expiry Date
Aug 25, 2026
Product Type
Clinical Chemistry Test System
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