Pure Global

AERTI Oxygen Concentrator - Indonesia BPOM Medical Device Registration

AERTI Oxygen Concentrator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403918837. The device is manufactured by SHENYANG AERTI TECH CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MANDIRI NUGRAHA AJITUNGGAL.

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 : B
AERTI Oxygen Concentrator
Analysis ID: AKL 20403918837

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MANDIRI NUGRAHA AJITUNGGAL

AR Address

Jl. Mangga Dua Raya, Komplek Bahan Bangunan Blok. F2 No.17 10730

Registration Date

Dec 27, 2019

Expiry Date

Feb 12, 2024

Product Type

Therapeutic Anesthesia Equipment

Portable oxygen generator.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing