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Auro Octane - Indonesia BPOM Medical Device Registration

Auro Octane is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31204321073. The device is manufactured by AUROLAB from India, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is MAIN INDEPENDENT MEDEQ.

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.

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BPOM Registered
Risk Class Kelas Resiko : D
Auro Octane
Analysis ID: AKL 31204321073

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

AUROLAB

Country of Origin

India

Authorized Representative

MAIN INDEPENDENT MEDEQ

AR Address

Ruko Graha Mas Pemuda Blok AC-19 jL. Pemuda Blok AC-19 Jl. Pemuda Kel. Jati Kec. Pulo Gadung Jakarta Timur

Registration Date

Oct 26, 2023

Expiry Date

Dec 03, 2025

Product Type

Therapeutic Eye Equipment

Intraocular fluid

Non Electromedic Sterile

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