MPHI - Indonesia BPOM Medical Device Registration
MPHI is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603810580. The device is manufactured by ASA LASER S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MULTIGUNA CIPTASENTOSA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ASA LASER S.R.L.Country of Origin
Italy
Authorized Representative
PT. MULTIGUNA CIPTASENTOSAAR Address
Surapati Core Blok M No.1 Jl. Phh. Mustofa No. 39 Bandung 022-87241400
Registration Date
Dec 27, 2022
Expiry Date
Dec 15, 2024
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
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