BIOSYNEX Ampliquick Sample Treatment - Indonesia BPOM Medical Device Registration
BIOSYNEX Ampliquick Sample Treatment is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10302320310. The device is manufactured by BIOSYNEX SA from France, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PACIFIC SAINTIFINDO.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
BIOSYNEX SACountry of Origin
France
Authorized Representative
PT. PACIFIC SAINTIFINDOAR Address
PASIFIK SAINTIFINDO
Registration Date
Jun 01, 2023
Expiry Date
Sep 07, 2024
Product Type
Microbiology Equipment
Transport culture medium.
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