MYO Quantitative Diagnostic Kit - Indonesia BPOM Medical Device Registration
MYO Quantitative Diagnostic Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305125220. The device is manufactured by BIOSCIENCE (TIANJIN) DIAGNOSTIC TECHNOLOGY CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PRATAMINDO MITRA RIZKY.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
China
Authorized Representative
PRATAMINDO MITRA RIZKYAR Address
Perumahan Bogorami Indah Regency, Jl. Bulak Setro Indah II Blok B 51-52, Surabaya
Registration Date
Aug 25, 2021
Expiry Date
Dec 31, 2024
Product Type
Immunological Test System
Myoglobin immunological test system.
Invitro Diagnostics
