AIM TSH Q Rapid Test - Indonesia BPOM Medical Device Registration
AIM TSH Q Rapid Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101221020. 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
Jul 21, 2022
Expiry Date
Jul 14, 2025
Product Type
Clinical Chemistry Test System
Thyroid stimulating hormone test system (kit & cair)
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