SLIDE. CHEMILUX Syphilis From - Indonesia BPOM Medical Device Registration
SLIDE. CHEMILUX Syphilis From is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303918685. The device is manufactured by DIA.PRO DIAGNOSTIC BIOPROBES S.R.L from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SAKEFA.
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DIA.CHEMILUX Syphilis Ab
Risk Classification
Product Class
Kelas : 2
Manufacturer
DIA.PRO DIAGNOSTIC BIOPROBES S.R.LCountry of Origin
Italy
Authorized Representative
PT. SAKEFAAR Address
Jl. Cireunde Raya No.26 Kel. Cireunde Kec. Ciputat Timur
Registration Date
Jan 17, 2020
Expiry Date
Sep 24, 2024
Product Type
Serological Reagents
Treponema pallidum treponemal test reagents.
Invitro Diagnostics
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DAY Validation Control
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DAY Anti-B (LB-2)
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DAY Anti-D (DVI-) (TH-28)
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SET DAYcells A1, B
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DAY Set Day Cells I-II-III
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