COMBIWIDAL 'BH' Antigen Slide & Tube Test Method - Indonesia BPOM Medical Device Registration
COMBIWIDAL 'BH' Antigen Slide & Tube Test Method is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303220562. The device is manufactured by GENUINE BIOSYSTEM PVT LMT. from India, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is RAJAERBA INDOCHEM.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GENUINE BIOSYSTEM PVT LMT.Country of Origin
India
Authorized Representative
RAJAERBA INDOCHEMAR Address
Jl. Hj. Tutty Alawiyah No. 8, Desa/Kelurahan Duren Tiga, Kec. Pancoran, Kota Adm. Jakarta Selatan, Provinsi DKI Jakarta, Kode Pos: 12760
Registration Date
Nov 19, 2024
Expiry Date
Sep 23, 2029
Product Type
Serological Reagents
Salmonella spp. serological reagents.
Invitro Diagnostics
REIGED DIAGNOSTICS Anti-D Monoclonal
REIGED DIAGNOSTICS Anti-AB Monoclonal
REIGED DIAGNOSTICS Anti-B Monoclonal
REIGED DIAGNOSTICS Anti-A Monoclonal
COMBIWIDAL 'CH' Antigen Slide & Tube Test Method
COMBIWIDAL 'H' Antigen Slide & Tube Test Method
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COMBIWIDAL 'AH' Antigen Slide & Tube Test Method
COMBIWIDAL 'AO' Antigen Slide & Tube Test Method
COMBIWIDAL 'BO' Antigen Slide & Tube Test Method
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