RESONANCE R16M - Indonesia BPOM Medical Device Registration
RESONANCE R16M is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20701420036. 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 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
Oct 07, 2024
Expiry Date
Dec 31, 2026
Product Type
Diagnostic Ear, Nose and Throat Equipment
Audiometer.
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