SOPHONIX D-Dimer Test Kit - Indonesia BPOM Medical Device Registration
SOPHONIX D-Dimer Test Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207220108. The device is manufactured by SOPHONIX CO.,LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is GOLDEN MEDIKA MANDIRI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SOPHONIX CO.,LTDCountry of Origin
China
Authorized Representative
GOLDEN MEDIKA MANDIRIAR Address
Jl. Raya Kalirungkut 27 Blok C-65
Registration Date
Jul 27, 2022
Expiry Date
Mar 10, 2027
Product Type
Haematology Package and Kit
Fibrinogen/fibrin degradation products assay.
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