RESONANCE Clinical Combined Middle Ear Analyzer - Indonesia BPOM Medical Device Registration
RESONANCE Clinical Combined Middle Ear Analyzer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20701516330. 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 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
HEARING VISIONAR Address
Darmawangsa Square Lantai 3 No.52 Jl. Darmawangsa VI & IX, Kelurahan Pulo Kecamatan Kebayoran Baru Jakarta Selatan
Registration Date
Sep 10, 2023
Expiry Date
Dec 31, 2026
Product Type
Diagnostic Ear, Nose and Throat Equipment
Audiometer.
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