BERNAFON LX 3 - Indonesia BPOM Medical Device Registration
BERNAFON LX 3 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20702420054. The device is manufactured by SBO HEARING 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
SBO HEARING A/SCountry of Origin
Denmark
Authorized Representative
PT. HEARING AIDS INDONESIAAR Address
Jl. Salemba Raya No 34-36A, Komp. Salemba Mas
Registration Date
May 07, 2024
Expiry Date
May 31, 2028
Product Type
Prosthetic Ear, Nose and Throat Equipment
Wireless air-conduction hearing aid
Non Radiation Electromedics
OTICON MORE 1 MINIBTE R
OTICON MORE 1 MINIBTE T
ESTONIAN 1
OTICON ZIRCON 2 MINIRITE R
OTICON ZIRCON 2 MINIBTE R
OTICON ZIRCON 2 MINIBTE T
OTICON ZIRCON 1 MINIRITE R
BERNAFON Viron 3
BERNAFON Viron 1
OTICON ZIRCON 1 MINIBTE R
ESTONIAN 1
SBO HEARING A/S
BERNAFON Viron 3
SBO HEARING A/S
BERNAFON Viron 1
SBO HEARING A/S
BERNAFON LX 7
SBO HEARING A/S
ReSound KE177-DW
GN RESOUND 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

