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AVENTA M Lung Ventilator - Indonesia BPOM Medical Device Registration

AVENTA M Lung Ventilator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403613010. The device is manufactured by JSC URAL INSTRUMENT ENGINEERING PLANT. from Russian Federation, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ANDIARTA MARTA UTAMA.

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 : C
AVENTA M Lung Ventilator
Analysis ID: AKL 20403613010

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Russian Federation

Authorized Representative

PT. ANDIARTA MARTA UTAMA

AR Address

Pusat Niaga Duta Mas Blok C2 No. 11-12 Jl. RS Fatmawati 39

Registration Date

Mar 18, 2020

Expiry Date

Jan 24, 2025

Product Type

Therapeutic Anesthesia Equipment

Continuous ventilator.

Non Radiation Electromedics

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