Pure Global

ILLUSTRO O2 - Indonesia BPOM Medical Device Registration

ILLUSTRO O2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204220468. The device is manufactured by INTEROJO from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ALFA INTERNAL OPTINDO.

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
ILLUSTRO O2
Analysis ID: AKL 21204220468

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

INTEROJO

Country of Origin

Korea

Authorized Representative

PT. ALFA INTERNAL OPTINDO

AR Address

Jalan Karel Satsuit Tubun Nomor 72 Lantai 1, RT/RW. 001/001 Kel. Slipi, Kec. Palmerah, Jakarta Barat, Prov. DKI Jakarta

Registration Date

Dec 15, 2022

Expiry Date

Dec 15, 2025

Product Type

Therapeutic Eye Equipment

Soft (hydrophilic) contact lens.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing