EME Iontophoresis and Electrostimulation - Indonesia BPOM Medical Device Registration
EME Iontophoresis and Electrostimulation is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403512921. The device is manufactured by EME S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. AGINTA SURGICALINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
EME S.R.L.Country of Origin
Italy
Authorized Representative
PT. AGINTA SURGICALINDOAR Address
Jalan Rawa Bambu Raya No. 88 R, RT. 013/005, Kel. Pasar Minggu, Kec. Pasar Minggu, Jakarta Selatan
Registration Date
Nov 06, 2020
Expiry Date
Dec 31, 2023
Product Type
Therapeutic Physical Health Equipment
Iontophoresis device.
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