VITROS Immunodiagnostic Products CA 19-9 ™ Reagent Pack - Indonesia BPOM Medical Device Registration
VITROS Immunodiagnostic Products CA 19-9 ™ Reagent Pack is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20306320198. The device is manufactured by FUJIREBIO DIAGNOSTICS, INC from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is EMERALINDO ASIA PACIFIC.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FUJIREBIO DIAGNOSTICS, INCCountry of Origin
United States
Authorized Representative
EMERALINDO ASIA PACIFICAR Address
RUKAN PERMATA SENAYAN BLOK G15, Lantai 1, JL.TENTARA PELAJAR NO. 5, Desa/Kelurahan Grogol Utara, Kec. Kebayoran Lama, Kota Adm. Jakarta Selatan, Provinsi DKI Jakarta Kode Pos: 12210
Registration Date
Nov 15, 2023
Expiry Date
Feb 24, 2028
Product Type
Tumor Antigen Immunologic Test System
Tumor-associated antigen immunological test system.
Invitro Diagnostics
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