BIOREX RF Latex Test - Indonesia BPOM Medical Device Registration
BIOREX RF Latex Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305420299. 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 SEGMED DISTRIBUTION INDONESIA.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
BIOREX DIAGNOSTICS LTD.Country of Origin
United Kingdom
Authorized Representative
SEGMED DISTRIBUTION INDONESIAAR Address
SEGMED DISTRIBUSI INDONESIA
Registration Date
Jun 28, 2024
Expiry Date
May 12, 2025
Product Type
Immunological Test System
Rheumatoid factor immunological test system.
Invitro Diagnostics
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BIOREX Pregnancy Latex Tests
BIOREX CRP Latex Test
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BIOREX ASO Latex Test
BIOREX Anti-AB Monoclonal
BIOREX Anti-A Monoclonal
BIOREX Anti-B Monoclonal
BIOREX Anti-D IgG/IgM Blend
FREND TSH Neo
NANOENTEK INC
LABType PE Conjugated Streptavidin
ONE LAMBDA INC.
BIOREX AHG Coomb's
BIOREX DIAGNOSTICS LTD.
BIOREX Serological Albumin 22 %
BIOREX DIAGNOSTICS LTD.
AKLIDES ANA Plus
MEDIPAN GMBH
RespiFinder 2SMART
PATHOFINDER B.V.
BIOREX Pregnancy Latex Tests
BIOREX DIAGNOSTICS LTD.
ANA 18 Line
GA GENERIC ASSAYS GMBH
BIOREX ASO Latex Test
BIOREX DIAGNOSTICS LTD.
BIOREX Anti-A Monoclonal
BIOREX DIAGNOSTICS LTD.

