RENDER Functional Fibrinogen Assay (Coagulation Method) - Indonesia BPOM Medical Device Registration
RENDER Functional Fibrinogen Assay (Coagulation Method) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207320253. The device is manufactured by RENDER BIOTECH CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FAITHFUL MEDICAL GRACE.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
RENDER BIOTECH CO., LTDCountry of Origin
China
Authorized Representative
PT. FAITHFUL MEDICAL GRACEAR Address
Mitra Sunter Boulevard Blok B No.39 Jl. Yos Sudarso Kav. 89
Registration Date
Mar 11, 2023
Expiry Date
Aug 22, 2025
Product Type
Haematology Package and Kit
Fibrinogen/fibrin degradation products assay.
Invitro Diagnostics
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