MD PACIFIC Fibrinogen (FIB) Assay Kit (Coagulation) - Indonesia BPOM Medical Device Registration
MD PACIFIC Fibrinogen (FIB) Assay Kit (Coagulation) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207125882. The device is manufactured by MD PACIFIC (TIANJIN) BIOTECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SUMIFIN CITRA ABADI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MD PACIFIC (TIANJIN) BIOTECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
PT. SUMIFIN CITRA ABADIAR Address
Jl. Alam Sutera Boulevard Alam Sutera Town Center (ASTC) Blok 10D No.19, Kel. Pakulonan, Kec. Serpong Utara - Tangerang Selatan 15325
Registration Date
Oct 27, 2023
Expiry Date
Jul 06, 2028
Product Type
Haematology Package and Kit
Fibrinogen/fibrin degradation products assay.
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