IOTest 3 Fixative Solution - Indonesia BPOM Medical Device Registration
IOTest 3 Fixative Solution is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204320547. The device is manufactured by IMMUNOTECH S.A.S., A BECKMAN COULTER COMPANY. from France, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is FOKUS DIAGNOSTIC INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
IMMUNOTECH S.A.S., A BECKMAN COULTER COMPANY.Country of Origin
France
Authorized Representative
FOKUS DIAGNOSTIC INDONESIAAR Address
Jl. Jatipadang Raya No.9A, RT.6/RW.4, Kelurahan Jatipadang, Kecamatan Pasar Minggu, Kota Jakarta Selatan, DKI Jakarta 12540
Registration Date
Dec 19, 2024
Expiry Date
Dec 31, 2027
Product Type
Reagents and Specimen Providers
General purpose reagent.
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