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AUSTAR BTE Hearing Aid - Indonesia BPOM Medical Device Registration

AUSTAR BTE Hearing Aid is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10702123858. The device is manufactured by AUSTAR HEARING SCIENCE AND TECHNOLOGY (XIAMEN) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. HEARING VISION.

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 : A
AUSTAR BTE Hearing Aid
Analysis ID: AKL 10702123858

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. HEARING VISION

AR Address

DARMAWANGSA SQUARE THE CITY WALK LT.3 UNIT 52, Jl. DARMAWANGSA VI DAN IX Kel. Pulo, Kec. Kebayoran Baru, Kota Adm. Jakarta Selatan 12160, Prov DKI Jakarta

Registration Date

Dec 20, 2024

Expiry Date

Jan 01, 2027

Product Type

Prosthetic Ear, Nose and Throat Equipment

Air-conduction hearing aid.

Non Radiation Electromedics

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