AIM Beta (β) - hCG Q Rapid Test - Indonesia BPOM Medical Device Registration
AIM Beta (β) - hCG Q Rapid Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101125436. 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. F5 & F6, JL. GAJAH MADA NO. 3-5
Registration Date
Apr 01, 2024
Expiry Date
Aug 16, 2026
Product Type
Clinical Chemistry Test System
Human chorionic gonadotropin (HCG) test system (card)
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