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ABDI Hearing Aid - Indonesia BPOM Medical Device Registration

ABDI Hearing Aid is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20702320104. The device is manufactured by HUIZHOU JINGHAO MEDICAL TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. HEARING AIDS INDONESIA.

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 : B
ABDI Hearing Aid
Analysis ID: AKL 20702320104

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. HEARING AIDS INDONESIA

AR Address

Sentra Salemba Mas Kav. A Jl. Salemba Raya No. 34-36 Kenari, Senen, Jakarta Pusat

Registration Date

Feb 10, 2023

Expiry Date

Aug 10, 2027

Product Type

Prosthetic Ear, Nose and Throat Equipment

(Deleted) Hearing Aid

Non Radiation Electromedics

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