Pure Global

SERENITY Hearing Aid - Indonesia BPOM Medical Device Registration

SERENITY Hearing Aid is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10702711524. The device is manufactured by XIAMEN NEWSOUND TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is SERENITY 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : A
SERENITY Hearing Aid
Analysis ID: AKL 10702711524

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

SERENITY INDONESIA

AR Address

Komp. Ruko Griya Inti Sentosa Jl. Griya Agung Blok O No. 96 Sunter

Registration Date

Dec 21, 2020

Expiry Date

Aug 25, 2025

Product Type

Prosthetic Ear, Nose and Throat Equipment

(Deleted) Hearing Aid.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Similar Products (1)
Other products with the same name