SHANGHAI LONG ISLAND D-Dimer Assay Kit - Indonesia BPOM Medical Device Registration
SHANGHAI LONG ISLAND D-Dimer Assay Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207320374. The device is manufactured by SHANGHAI LONG ISLAND BIOTEC,CO.,LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MINDRAY MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHANGHAI LONG ISLAND BIOTEC,CO.,LTDCountry of Origin
China
Authorized Representative
PT. MINDRAY MEDICAL INDONESIAAR Address
Menara DEA II Lt.17, Jl. Mega Kuningan Barat Kav.E4.3 No.1-2, Kel. Kuningan Timur, Kec.Setiabudi Kawasan Mega Kuningan, Jakarta Selatan
Registration Date
Aug 14, 2023
Expiry Date
Oct 10, 2026
Product Type
Haematology Package and Kit
Fibrinogen/fibrin degradation products assay.
Invitro Diagnostics
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