AIM TB™ Rapid Card - Indonesia BPOM Medical Device Registration
AIM TB™ Rapid Card is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303220823. The device is manufactured by VEDA LAB from France, and is classified as Risk Class Kelas Resiko : C. 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
Nov 21, 2022
Expiry Date
Nov 21, 2025
Product Type
Serological Reagents
Mycobacterium tuberculosis immunofluorescent reagents.
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