BIOPHEN Rivaroxaban Plasma Calibrator - Indonesia BPOM Medical Device Registration
BIOPHEN Rivaroxaban Plasma Calibrator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208610832. The device is manufactured by HYPHEN BIOMED. from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SYSMEX INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
HYPHEN BIOMED.Country of Origin
France
Authorized Representative
PT. SYSMEX INDONESIAAR Address
Cyber 2 Tower, 5th Floor Unit E Jl. HR. Rasuna Said Blok X.5 No.13
Registration Date
Apr 29, 2024
Expiry Date
Aug 24, 2025
Product Type
Hematological Reagents
Calibrator for hemoglobin or hematocrit measurement.
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