BIOSYNEX DENGUE Ab BSS - Indonesia BPOM Medical Device Registration
BIOSYNEX DENGUE Ab BSS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303125469. The device is manufactured by BIOSYNEX S.A from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. NELTA MULTI GRACIA.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
BIOSYNEX S.ACountry of Origin
France
Authorized Representative
PT. NELTA MULTI GRACIAAR Address
Metland Menteng. Jl. Menteng Niaga Blok J7 No.1 Ujung Menteng, Cakung, Jakarta Timur 13960
Registration Date
Apr 10, 2023
Expiry Date
Feb 13, 2026
Product Type
Serological Reagents
Dengue virus serological reagents
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