ADVIA Centaur SYPH Ready Pack - Indonesia BPOM Medical Device Registration
ADVIA Centaur SYPH Ready Pack is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303122150. The device is manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC. (EAST WALPOLE) from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is SIEMENS HEALTHINEERS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
United States
Authorized Representative
SIEMENS HEALTHINEERS INDONESIAAR Address
Perkantoran Hijau Arkadia Tower F, Lantai 18, Jl. Tahi Bonar Simatupang Kav. 88, Kel. Kebagusan, Kec. Pasar Minggu, Jakarta Selatan, DKI Jakarta
Registration Date
Apr 16, 2021
Expiry Date
Mar 04, 2024
Product Type
Serological Reagents
Treponema pallidum nontreponemal test reagents.
Invitro Diagnostics
ADVIA Centaur Anti-HBs2 Quality Control (aHBs2 QC)
ADVIA Centaur Calibrator D
ADVIA Centaur VB12 Diluent Ready Pack
ADVIA Centaur SYPH Ready Pack
ADVIA Centaur Multi Diluent 10 ReadyPack
ADVIA Centaur HBc IgM Quality Control (aHBcM QC)
ADVIA Centaur Vitamin B12 (VB12)
ADVIA Centaur CA 125II Ready Pack
ADVIA Centaur CA 125II Calibrator
ADVIA Centaur T4 Ready Pack.
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ADVIA Centaur VB12 Diluent Ready Pack
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Dimension Phosphorus Flex (PHOS) reagent cartridge
SIEMENS HEALTHCARE DIAGNOSTICS INC.