Pure Global

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
BIOSYNEX DENGUE Ab BSS
Analysis ID: AKL 20303125469

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

BIOSYNEX S.A

Country of Origin

France

Authorized Representative

PT. NELTA MULTI GRACIA

AR 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

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from BIOSYNEX S.A
Products from the same manufacturer (1 products)