Pure Global

IMMUNEMED Dengue NS1 Ag Rapid - Indonesia BPOM Medical Device Registration

IMMUNEMED Dengue NS1 Ag Rapid is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303911833. The device is manufactured by IMMUNEMED, INC. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDISON JAYA RAYA.

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
IMMUNEMED Dengue NS1 Ag Rapid
Analysis ID: AKL 20303911833

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

IMMUNEMED, INC.

Country of Origin

Korea

Authorized Representative

PT. MEDISON JAYA RAYA

AR Address

JL. KAPT.P. TENDEAN NO.7, MAMPANG PRAPATAN

Registration Date

Mar 28, 2019

Expiry Date

Dec 31, 2023

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