EME Ionophoresis and Electrostimulation Therapy - Indonesia BPOM Medical Device Registration
EME Ionophoresis and Electrostimulation Therapy is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403913861. 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 AGINTA SURGICALINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
EME S.R.L.Country of Origin
Italy
Authorized Representative
AGINTA SURGICALINDOAR Address
Ruko Grand Pasar Minggu Jl. Rawa Bambu No. 88 R
Registration Date
Nov 28, 2023
Expiry Date
Dec 31, 2025
Product Type
Therapeutic Physical Health Equipment
Iontophoresis device.
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