Pure Global

AIM Dengue NS1 Antigen Rapid Test - Indonesia BPOM Medical Device Registration

AIM Dengue NS1 Antigen Rapid Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303125706. The device is manufactured by XIAMEN BOSON BIOTECH CO, LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ACCURATE INTAN MADYA.

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
AIM Dengue NS1 Antigen Rapid Test
Analysis ID: AKL 20303125706

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. ACCURATE INTAN MADYA

AR Address

KOMPLEK DUTA MERLIN, BLOK. F5 & F6, JL. GAJAH MADA NO. 3-5

Registration Date

Jul 03, 2024

Expiry Date

Jul 01, 2027

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