BIOREX Salmonella Paratyphi BO - Indonesia BPOM Medical Device Registration
BIOREX Salmonella Paratyphi BO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303420127. The device is manufactured by BIOREX DIAGNOSTICS LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : B. 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
Apr 05, 2024
Expiry Date
May 12, 2025
Product Type
Serological Reagents
Salmonella spp. serological reagents.
Invitro Diagnostics
BIOREX AHG Coomb's
BIOREX Serological Albumin 22 %
BIOREX Pregnancy Latex Tests
BIOREX RF Latex Test
BIOREX Rapid Plasma Reagen (RPR)
BIOREX CRP Latex Test
BIOREX Anti-AB Monoclonal
BIOREX ASO Latex Test
BIOREX Anti-B Monoclonal
BIOREX Anti-A Monoclonal
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