AIM TPHA™ Test - Indonesia BPOM Medical Device Registration
AIM TPHA™ Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303220798. The device is manufactured by NEWMARKET BIOMEDICAL, LTD from United Kingdom, 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
NEWMARKET BIOMEDICAL, LTDCountry of Origin
United Kingdom
Authorized Representative
PT. ACCURATE INTAN MADYAAR Address
Komplek Duta Merlin Blok F No.5-6. Jl.Gajah Mada No.3-5
Registration Date
Nov 16, 2022
Expiry Date
Nov 15, 2025
Product Type
Serological Reagents
Treponema pallidum nontreponemal test reagents.
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