LYSERCELL ™ WDF - Indonesia BPOM Medical Device Registration
LYSERCELL ™ WDF is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208020021. 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., LTD.Country 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
Mar 24, 2023
Expiry Date
Jan 16, 2028
Product Type
Hematological Reagents
Red cell lysing reagent.
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