UF-CELLPACK SF - Indonesia BPOM Medical Device Registration
UF-CELLPACK SF is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208420202. The device is manufactured by SYSMEX ASIA PACIFIC PTE LTD from Singapore, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SYSMEX INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SYSMEX ASIA PACIFIC PTE LTDCountry of Origin
Singapore
Authorized Representative
PT. SYSMEX INDONESIAAR Address
Cyber 2 Tower, 5th Floor Unit E Jl. HR. Rasuna Said Blok X.5 No.13
Registration Date
Aug 04, 2024
Expiry Date
Jan 16, 2028
Product Type
Hematological Reagents
Blood cell diluents
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