SEIMITSU Hematology Diluent - Indonesia BPOM Medical Device Registration
SEIMITSU Hematology Diluent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208420128. The device is manufactured by SHENZHEN HETO MEDICAL TECH CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SEIMITSU DIAGNOSTICS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHENZHEN HETO MEDICAL TECH CO., LTDCountry of Origin
China
Authorized Representative
PT. SEIMITSU DIAGNOSTICSAR Address
Harton Tower 7th Floor, Jl. Boulevard Artha Gading, Kel. Kelapa Gading Barat, Kec. Kelapa Gading, Jakarta Utara.
Registration Date
Jun 19, 2024
Expiry Date
Jan 30, 2027
Product Type
Hematological Reagents
Blood cell diluents
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