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.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GN RESOUND A/SCountry of Origin
Denmark
Authorized Representative
PT. HEARING AIDS INDONESIAAR 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
ESTONIAN 1
SBO HEARING A/S
BERNAFON Viron 3
SBO HEARING A/S
BERNAFON Viron 1
SBO HEARING A/S
BERNAFON LX 3
SBO HEARING A/S
BERNAFON LX 7
SBO HEARING A/S
JINGHAO Hearing Aid
HUIZHOU JINGHAO MEDICAL TECHNOLOGY CO., LTD.
ABDI Hearing Aid
HUIZHOU JINGHAO MEDICAL TECHNOLOGY CO., LTD.
ESTONIAN 5
DGS POLAND SP. Z.O.O
ESTONIAN 3
BERNAFON AT
LEOX 3
BERNAFON AT

