AQUIOS Flow-Count Fluorospheres - Indonesia BPOM Medical Device Registration
AQUIOS Flow-Count Fluorospheres is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207320285. The device is manufactured by BECKMAN COULTER, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FOCUS DIAGNOSTIC INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BECKMAN COULTER, INC.Country of Origin
United States
Authorized Representative
PT. FOCUS DIAGNOSTIC INDONESIAAR Address
Jl. Jatipadang Raya No.9A, RT.6/RW.4, Kelurahan Jatipadang, Kecamatan Pasar Minggu, Kota Jakarta Selatan, DKI Jakarta 12540
Registration Date
Apr 20, 2023
Expiry Date
Jun 01, 2025
Product Type
Haematology Package and Kit
Leukocyte alkaline phosphatase test.
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