VISTA V3-R - Indonesia BPOM Medical Device Registration
VISTA V3-R is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20702420014. The device is manufactured by SONOVA AT from Switzerland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. HEARING LIFE.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SONOVA ATCountry of Origin
Switzerland
Authorized Representative
PT. HEARING LIFEAR Address
Talavera Office Park Lantai 28 Suite M 3301 Jl. TB Simatupang Kav. 22-26
Registration Date
Feb 02, 2024
Expiry Date
Mar 31, 2028
Product Type
Prosthetic Ear, Nose and Throat Equipment
Wireless air-conduction hearing aid
Non Radiation Electromedics
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