RESONANCE Clinical Audiometer - Indonesia BPOM Medical Device Registration
RESONANCE Clinical Audiometer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20701717694. The device is manufactured by M.R.S S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. HEARING VISION.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
M.R.S S.R.L.Country of Origin
Italy
Authorized Representative
PT. HEARING VISIONAR Address
Darmawangsa Square Lantai 3 No.52 Jl. Darmawangsa VI & IX, Kelurahan Pulo Kecamatan Kebayoran Baru Jakarta Selatan
Registration Date
Oct 17, 2023
Expiry Date
Dec 31, 2026
Product Type
Diagnostic Ear, Nose and Throat Equipment
Audiometer.
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