MD PACIFIC Coagulation Quality Control Plasma Kit (Coagulation) - Indonesia BPOM Medical Device Registration
MD PACIFIC Coagulation Quality Control Plasma Kit (Coagulation) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20205026022. The device is manufactured by MD PACIFIC (TIANJIN) BIOTECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. 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., LTDCountry 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
Nov 15, 2023
Expiry Date
Jul 07, 2028
Product Type
Automatic and Semi-Automatic Hematology Equipment
Multipurpose system for in vitro coagulation studies (for reagent & control)
Invitro Diagnostics
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