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ReSound KE177-DW - Indonesia BPOM Medical Device Registration

ReSound KE177-DW is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20702320127. The device is manufactured by GN RESOUND A/S from Denmark, 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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Risk Class Kelas Resiko : B
ReSound KE177-DW
Analysis ID: AKL 20702320127

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

GN RESOUND A/S

Country of Origin

Denmark

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

May 19, 2023

Expiry Date

Oct 21, 2025

Product Type

Prosthetic Ear, Nose and Throat Equipment

(Deleted) Hearing Aid

Non Radiation Electromedics

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