HUMASIS HUBI D-DIMER - Indonesia BPOM Medical Device Registration
HUMASIS HUBI D-DIMER is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207914525. The device is manufactured by HUMASIS CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is INDOCORE PERKASA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HUMASIS CO., LTD.Country of Origin
Korea
Authorized Representative
INDOCORE PERKASAAR Address
Komplek Graha Mas Pemuda Blok AB No. 19, Jl. Pemuda RT 020 / RW 006 Kel. Jati, Kec. Pulo Gadung, Jakarta Timur, DKI Jakarta
Registration Date
Jan 19, 2021
Expiry Date
Nov 18, 2025
Product Type
Haematology Package and Kit
Fibrinogen/fibrin degradation products assay.
Invitro Diagnostics
HUMASIS Malaria P.f/Pan Antigen Test
HUBI-QUAN Pro and Accessories
HUBI-TAS and Accessories
HUMASIS COVID-19 Ag Test
HUMASIS Covid-19 IgG/IgM Test
HUBI Cardiac DUO (TnI/CK-MB)
HUMASIS Dengue IgG/IgM Antibody Test
HUMASIS Dengue Combo Test
HUBI CRP
HUBI 3-in-1 (B) TnI/BNP/CK-MB
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