VivaDiag Triiodothyronine Test Kit FIA - Indonesia BPOM Medical Device Registration
VivaDiag Triiodothyronine Test Kit FIA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101122602. The device is manufactured by VIVACHEK BIOTECH (HANGZHOU) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MAIN MEDICAL CHAKRA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
VIVACHEK BIOTECH (HANGZHOU) CO., LTD.Country of Origin
China
Authorized Representative
PT. MAIN MEDICAL CHAKRAAR Address
FORESTA BUSINESS LOFT 6 No. 10, Jl. Raya Boulevard Utara BSD City, Desa/Kelurahan Lengkong Kulon
Registration Date
Jun 21, 2023
Expiry Date
Sep 01, 2025
Product Type
Clinical Chemistry Test System
Triiodothyronine uptake test system (card)
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