YUMIZEN G200 - Indonesia BPOM Medical Device Registration
YUMIZEN G200 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20205918689. The device is manufactured by DIAGON LTD. from Hungary, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. HORIBA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DIAGON LTD.Country of Origin
Hungary
Authorized Representative
PT. HORIBA INDONESIAAR Address
Jl. Jalur Sutera , Blok. 20A, No. 16 - 17, Kel. Kunciran, Kec. Pinang
Registration Date
Dec 30, 2019
Expiry Date
Jan 30, 2024
Product Type
Automatic and Semi-Automatic Hematology Equipment
Coagulation instrument.
Invitro Diagnostics
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