BEURER Hearing Amplifier - Indonesia BPOM Medical Device Registration
BEURER Hearing Amplifier is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10702612562. The device is manufactured by BEURER GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SERENITY INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
BEURER GMBHCountry of Origin
Germany
Authorized Representative
PT. SERENITY INDONESIAAR Address
Komplek Ruko Permata Kota Blok Q No. 10 Jl. Pangeran Tubagus Angke No.170 RT.010 RW . 01
Registration Date
Oct 04, 2023
Expiry Date
Mar 31, 2026
Product Type
Prosthetic Ear, Nose and Throat Equipment
(Deleted) Hearing Aid.
Non Radiation Electromedics
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