Pure Global

EZiTELL HIV 1. 2 Rapid Test Cassette - Indonesia BPOM Medical Device Registration

EZiTELL HIV 1. 2 Rapid Test Cassette is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30305420247. The device is manufactured by HANGZHOU ALL TEST BIOTECH CO., LTD from China, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is MAIN ONCOPROBE.

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
EZiTELL HIV 1. 2 Rapid Test Cassette
Analysis ID: AKL 30305420247

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

China

Authorized Representative

MAIN ONCOPROBE

AR Address

Apartemen Istana Harmoni Plaza Kompleks Harmoni Plaza, Jl. Suryopranoto 2 Unit 1M dan 2K, RT 2 RW 8 Desa/Kel. Gambir, Kec. Gambir, Kota AdmJakarta Pusat, Provinsi DKI Jakarta Kode Pos 10130

Registration Date

Jun 05, 2024

Expiry Date

Jan 24, 2029

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