BIOMAJESTY LDH FS IFCC - Indonesia BPOM Medical Device Registration
BIOMAJESTY LDH FS IFCC is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101020507. The device is manufactured by DIASYS DIAGNOSTIC SYSTEMS, GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SYSMEX INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DIASYS DIAGNOSTIC SYSTEMS, GMBHCountry of Origin
Germany
Authorized Representative
SYSMEX INDONESIAAR Address
Cyber 2 Tower, 5th Floor Unit E Jl. HR. Rasuna Said Blok X.5 No.13
Registration Date
Dec 15, 2021
Expiry Date
Sep 17, 2026
Product Type
Clinical Chemistry Test System
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TruLab Urine Level 2
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TruLab Urine Level 1
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