AQUIOS CL Flow Cytometer - Indonesia BPOM Medical Device Registration
AQUIOS CL Flow Cytometer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20205024290. 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
18 Office Park, Tower A, Jl. TB Simatupang No.18 MZ Floor, Unit D1-A/89, Kelurahan Kebagusan
Registration Date
Aug 23, 2022
Expiry Date
Jun 01, 2025
Product Type
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