BIOREX Rapid Plasma Reagen (RPR) - Indonesia BPOM Medical Device Registration
BIOREX Rapid Plasma Reagen (RPR) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303420274. The device is manufactured by BIOREX DIAGNOSTICS LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SEGMED DISTRIBUTION INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BIOREX DIAGNOSTICS LTD.Country of Origin
United Kingdom
Authorized Representative
PT. SEGMED DISTRIBUTION INDONESIAAR Address
SEGMED DISTRIBUSI INDONESIA
Registration Date
Jun 28, 2024
Expiry Date
May 12, 2025
Product Type
Serological Reagents
Treponema pallidum nontreponemal test reagents.
Invitro Diagnostics
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BIOREX Anti-A Monoclonal
BIOREX Anti-D IgG/IgM Blend
BIOREX ASO Latex Test
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