INNO-LiPA Mycobacteria v2 Amp <20T, CE> - Indonesia BPOM Medical Device Registration
INNO-LiPA Mycobacteria v2 Amp <20T, CE> is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303915277. The device is manufactured by FUJIREBIO EUROPE N.V. from Belgium, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ANDAMAN MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FUJIREBIO EUROPE N.V.Country of Origin
Belgium
Authorized Representative
PT. ANDAMAN MEDICAL INDONESIAAR Address
Komplek Rukan Kirana Blok B No. 10, Jalan DI Panjaitan, Jakarta Timur
Registration Date
Aug 16, 2019
Expiry Date
Jan 11, 2024
Product Type
Serological Reagents
Mycobacterium tuberculosis immunofluorescent reagents.
Invitro Diagnostics
INNO-LiPA HPV Genotyping Extra II Amp <20T, CE>
INNO-LiPA HPV Genotyping Extra II <20T,CE>
INNO-LIA HIV I/II Score
INNOTEST ฮฒ-AMYLOID(1-40)
INNOTEST PHOSPHO-TAU (181P)
INNO-LIA HCV Score
INNOTEST ฮฒ-AMYLOID(1-42)
INNOTEST hTau Ag
Tendigo
LiRAS for LiPA HPV v3
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