Pure Global

ALCORE Dengue NS1 Rapid Test Cassette - Indonesia BPOM Medical Device Registration

ALCORE Dengue NS1 Rapid Test Cassette is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303420304. The device is manufactured by HANGZHOU ALLTEST BIOTECH CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRIMITRA DIAGNOSTICS INDONESIA.

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
ALCORE Dengue NS1 Rapid Test Cassette
Analysis ID: AKL 20303420304

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. TRIMITRA DIAGNOSTICS INDONESIA

AR Address

JL. PANGERAN JAYAKARTA, RUKAN BUNTU WARGA NO.23A KEL.MANGGA DUA SELATAN KEC. SAWAH BESAR, JAKARTA PUSAT

Registration Date

Jul 07, 2024

Expiry Date

Jul 05, 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