SIEMENS N Antiserum to Human C4 - Indonesia BPOM Medical Device Registration
SIEMENS N Antiserum to Human C4 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305220094. 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 SIEMENS HEALTHINEERS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBHCountry of Origin
Germany
Authorized Representative
SIEMENS HEALTHINEERS INDONESIAAR Address
Perkantoran Hijau Arkadia Tower F, Lantai 18, Jl.Tahi Bonar Simatupang Kav. 88
Registration Date
Jan 25, 2024
Expiry Date
Oct 19, 2026
Product Type
Immunological Test System
Complement components immunological test system.
Invitro Diagnostics
IMMULITE Probe Wash Module
N Latex ADnase B
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SIEMENS N Antiserum to Human Fibrinogen
SIEMENS N Protein Control LC1
SIEMENS N Sample Diluent
SIEMENS N Antiserum to Human Antithrombin III
SIEMENS N/T N Latex Ferritin
SIEMENS N Antiserum to Human Hemopexin
SIEMENS N Latex IgE mono
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