VIVOSONIC Integrity Auditory Diagnostic System - Indonesia BPOM Medical Device Registration
VIVOSONIC Integrity Auditory Diagnostic System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20701220001. The device is manufactured by VIVOSONIC INC. from Canada, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is HEARING VISION.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
VIVOSONIC INC.Country of Origin
Canada
Authorized Representative
HEARING VISIONAR Address
DARMAWANGSA SQUARE THE CITY WALK LT.3 UNIT 52, Jl. DARMAWANGSA VI DAN IX Kel. Pulo, Kec. Kebayoran Baru, Kota Adm. Jakarta Selatan 12160, Prov DKI Jakarta
Registration Date
Feb 22, 2024
Expiry Date
Jan 22, 2027
Product Type
Diagnostic Ear, Nose and Throat Equipment
Audiometer.
Non Radiation Electromedics
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