BERICHROM Plasminogen - Indonesia BPOM Medical Device Registration
BERICHROM Plasminogen is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207905010. The device is manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. 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
Oct 24, 2022
Expiry Date
Mar 16, 2027
Product Type
Haematology Package and Kit
Fibrinogen/fibrin degradation products assay.
Invitro Diagnostics
IMMULITE Probe Wash Module
N Latex ADnase B
SIEMENS N Protein Control LC1
SIEMENS N Antiserum to Human Fibrinogen
SIEMENS N Protein Control LC2
SIEMENS N Antiserum to Human Antithrombin III
SIEMENS N Sample Diluent
SIEMENS N/T N Latex Ferritin
SIEMENS N Latex IgE mono
SIEMENS N Antiserum to Human Hemopexin
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