Pure Global

ICHROMA™ Dengue NS1 Ag - Indonesia BPOM Medical Device Registration

ICHROMA™ Dengue NS1 Ag is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303321236. The device is manufactured by BODITECH WITH INC. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ZOE PELITA NUSANTARA.

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
ICHROMA™ Dengue NS1 Ag
Analysis ID: AKL 20303321236

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

BODITECH WITH INC.

Country of Origin

Korea

Authorized Representative

PT. ZOE PELITA NUSANTARA

AR Address

Jl. Cikini II No. 8B Menteng

Registration Date

Jul 03, 2023

Expiry Date

Oct 01, 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