Pure Global

BIOEASY ™ ONE STEP Dengue NS1 Ag Rapid Test - Indonesia BPOM Medical Device Registration

BIOEASY ™ ONE STEP Dengue NS1 Ag Rapid Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303918284. The device is manufactured by SHENZHEN BIOEASY BIOTECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. LANIROS DIAN PHARMA.

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
BIOEASY ™ ONE STEP Dengue NS1 Ag Rapid Test
Analysis ID: AKL 20303918284

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. LANIROS DIAN PHARMA

AR Address

GEDUNG SATRIO TOWER LT. 22, JL. PROF. DR. SATRIO KAV. C4

Registration Date

Dec 12, 2019

Expiry Date

Jun 20, 2024

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