SIEMENS Fibrinogen Calibrator Kit - Indonesia BPOM Medical Device Registration
SIEMENS Fibrinogen Calibrator Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207902656. 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 GMBH.Country 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
Jul 26, 2022
Expiry Date
Mar 16, 2027
Product Type
Haematology Package and Kit
Fibrinogen determination system.
Invitro Diagnostics
N Antiserum Human Albumin
SIEMENS N Latex Lp(a) Reagent
SIEMENS N Latex Beta 2–Microglobulin
SIEMENS HEALTHINEERS N Protein Standard SL
SIEMENS N FLC Standard SL
SIEMENS N Latex sTfR
SIEMENS N Reaction Buffer
SIEMENS N Antiserum to Human IgG
SIEMENS N FLC Supplementary Reagent
SIEMENS N/T Protein Control SL/M
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