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RESOUND ENYA BTE Hearing Aid - Indonesia BPOM Medical Device Registration

RESOUND ENYA BTE Hearing Aid is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20702023735. 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. NOBEL JAYA MANDIRI.

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BPOM Registered
Risk Class Kelas Resiko : B
RESOUND ENYA BTE Hearing Aid
Analysis ID: AKL 20702023735

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

GN RESOUND A/S

Country of Origin

Denmark

Authorized Representative

PT. NOBEL JAYA MANDIRI

AR Address

Jalan Terusan Kelapa Hibrida Blok C-08 RT.004 RW.011 Kel. Sukapura Kec. Cilincing

Registration Date

Jul 09, 2020

Expiry Date

Jan 01, 2025

Product Type

Prosthetic Ear, Nose and Throat Equipment

Wireless air-conduction hearing aid

Non Radiation Electromedics

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