AIM CRP Q Rapid Test - Indonesia BPOM Medical Device Registration
AIM CRP Q Rapid Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20305220302. 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
Aug 15, 2022
Expiry Date
Aug 02, 2025
Product Type
Immunological Test System
C-reactive protein immunological test system.
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