VITROS Immunodiagnostic Products Toxoplasma IgM Reagent Pack - Indonesia BPOM Medical Device Registration
VITROS Immunodiagnostic Products Toxoplasma IgM Reagent Pack is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303320952. The device is manufactured by ORTHO-CLINICAL DIAGNOSTICS from United Kingdom, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. EMERALINDO ASIA PACIFIC.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ORTHO-CLINICAL DIAGNOSTICSCountry of Origin
United Kingdom
Authorized Representative
PT. 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
May 21, 2024
Expiry Date
Feb 24, 2028
Product Type
Serological Reagents
Toxoplasma gondii serological reagents.
Invitro Diagnostics
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VITROS Immunodiagnostic Products Anti-HBc IgM Reagent Pack
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