YUMIZEN G400 DDi - Indonesia BPOM Medical Device Registration
YUMIZEN G400 DDi is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20205918688. The device is manufactured by DIAGON LTD. from Hungary, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is HORIBA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DIAGON LTD.Country of Origin
Hungary
Authorized Representative
HORIBA INDONESIAAR Address
Jl. Jalur Sutera , Blok. 20A, No. 16 - 17, Kel. Kunciran, Kec. Pinang
Registration Date
Feb 01, 2024
Expiry Date
Nov 30, 2028
Product Type
Automatic and Semi-Automatic Hematology Equipment
Coagulation instrument.
Invitro Diagnostics
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Yumizen CR CHOLESTEROL
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Yumizen CR BILIRUBIN TOTAL
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Yumizen CR BILIRUBIN DIRECT
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Yumizen CR GPT (TOOL)
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Yumizen CR URIC ACID
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Yumizen CR TRIGLYCERIDES
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Yumizen CR Creatinine
HORIBA INDIA PRIVATE LIMITED

