BEURER Digital Hearing Amplifiers - Indonesia BPOM Medical Device Registration
BEURER Digital Hearing Amplifiers is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10702129989. The device is manufactured by BEURER GMBH. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is Serenity Indonesia.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
BEURER GMBH.Country of Origin
Germany
Authorized Representative
Serenity IndonesiaAR Address
Komp. Ruko Griya Inti Sentosa Jl. Griya Agung Blok O No. 96 Sunter
Registration Date
Dec 26, 2021
Expiry Date
Aug 20, 2025
Product Type
Prosthetic Ear, Nose and Throat Equipment
(Deleted) Hearing Aid.
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