SIEMENS N Antiserum to Human Fibrinogen - Indonesia BPOM Medical Device Registration
SIEMENS N Antiserum to Human Fibrinogen is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20207320312. 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. SIEMENS HEALTHINEERS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBHCountry of Origin
Germany
Authorized Representative
PT. SIEMENS HEALTHINEERS INDONESIAAR Address
Perkantoran Hijau Arkadia Tower F, Lantai 18, Jl.Tahi Bonar Simatupang Kav. 88
Registration Date
Sep 20, 2024
Expiry Date
Oct 19, 2026
Product Type
Haematology Package and Kit
Fibrinogen/fibrin degradation products assay.
Invitro Diagnostics
IMMULITE Probe Wash Module
SIEMENS N Protein Control LC2
SIEMENS N Protein Control LC1
N Latex ADnase B
SIEMENS N Antiserum to Human Antithrombin III
SIEMENS N Sample Diluent
SIEMENS N/T N Latex Ferritin
SIEMENS N Antiserum to Human Hemopexin
SIEMENS N Latex IgE mono
SIEMENS N Antiserum to Human Alpha-1-acid Glycoprotein
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