AIM T3 Elisa Test - Indonesia BPOM Medical Device Registration
AIM T3 Elisa Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101322413. The device is manufactured by VEDA LAB from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ACCURATE INTAN MADYA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
VEDA LABCountry of Origin
France
Authorized Representative
PT. ACCURATE INTAN MADYAAR Address
Komplek Duta Merlin Blok F No.5-6. Jl.Gajah Mada No.3-5
Registration Date
Jan 25, 2023
Expiry Date
Jan 16, 2026
Product Type
Clinical Chemistry Test System
Total triiodothyronine test system (kit & cair)
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