SIEMENS Control Plasma N - Indonesia BPOM Medical Device Registration
SIEMENS Control Plasma N is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208905087. The device is manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH from Germany, 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
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBHCountry of Origin
Germany
Authorized Representative
PT. SYSMEX INDONESIAAR Address
Cyber 2 Tower, 5th Floor Unit E Jl. HR. Rasuna Said Blok X.5 No.13
Registration Date
Aug 29, 2022
Expiry Date
Mar 16, 2027
Product Type
Hematological Reagents
Hematology quality control mixture.
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