HE. CHEMILUX HBsAg - Indonesia BPOM Medical Device Registration
HE. CHEMILUX HBsAg is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10305917812. The device is manufactured by DIA.PRO DIAGNOSTIC BIOPROBES S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SAKEFA.
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DIA.CHEMILUX HBsAg
Risk Classification
Product Class
Kelas : 1
Manufacturer
DIA.PRO DIAGNOSTIC BIOPROBES S.R.L.Country of Origin
Italy
Authorized Representative
PT. SAKEFAAR Address
Jl. Cireunde Raya No.26 Kel. Cireunde Kec. Ciputat Timur
Registration Date
Dec 06, 2019
Expiry Date
Sep 24, 2024
Product Type
Immunological Test System
Automated Bloodborne Pathogen test system
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