BIOREX Serological Albumin 22 % - Indonesia BPOM Medical Device Registration
BIOREX Serological Albumin 22 % is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209420431. 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.
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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
Nov 13, 2024
Expiry Date
May 12, 2025
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Blood group substances of nonhuman origin for in vitro diagnostic use.
Invitro Diagnostics
BIOREX AHG Coomb's
BIOREX Pregnancy Latex Tests
BIOREX RF Latex Test
BIOREX CRP Latex Test
BIOREX Rapid Plasma Reagen (RPR)
BIOREX Anti-AB Monoclonal
BIOREX ASO Latex Test
BIOREX Anti-B Monoclonal
BIOREX Anti-A 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.
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 RF Latex Test
BIOREX DIAGNOSTICS LTD.
BIOREX Anti-A Monoclonal
BIOREX DIAGNOSTICS LTD.
BIOREX Anti-AB Monoclonal
BIOREX DIAGNOSTICS LTD.