Pure Global

AIM HIV 1/2 Tripleline Rapid Test - Indonesia BPOM Medical Device Registration

AIM HIV 1/2 Tripleline Rapid Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30305220211. The device is manufactured by XIAMEN BOSON BIOTECH CO, LTD from China, and is classified as Risk Class Kelas Resiko : D. 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 : D
AIM HIV 1/2 Tripleline Rapid Test
Analysis ID: AKL 30305220211

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

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

Jan 23, 2025

Expiry Date

Jan 18, 2028

Product Type

Immunological Test System

Multiple autoantibodies immunological test system.

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing