COCHLEAR Kanso Sound Processor - Indonesia BPOM Medical Device Registration
COCHLEAR Kanso Sound Processor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10702715593. The device is manufactured by COCHLEAR LTD. from Australia, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is KASOEM HEARING.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
COCHLEAR LTD.Country of Origin
Australia
Authorized Representative
KASOEM HEARINGAR Address
Jl. Setiabudi No. 34, RT 002 RW 003, Kel. Hegarmanah, Kec. Cidadap, Kota Bandung, Jawa Barat
Registration Date
Dec 18, 2023
Expiry Date
Aug 31, 2028
Product Type
Prosthetic Ear, Nose and Throat Equipment
(Deleted) Hearing Aid.
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