EME Ultrasound Therapy - Indonesia BPOM Medical Device Registration
EME Ultrasound Therapy is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403512288. 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
Jalan Rawa Bambu Raya No. 88 R, RT. 013/005, Kel. Pasar Minggu, Kec. Pasar Minggu, Jakarta Selatan
Registration Date
Oct 29, 2020
Expiry Date
Dec 31, 2023
Product Type
Therapeutic Physical Health Equipment
Ultrasonic diathermy.
Non Radiation Electromedics
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EME Combine Electro and Ultrasound Therapy
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EME Ultrasound Therapy
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EME ENDODIATHERMY
EME S.R.L.
EME Diathermy Therapy
EME SRL
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EME SRL
EME Combined Electro, Ultrasound, Magnetic and Laser
EME SRL.
EME Shock Wave Therapy
EME SRL
EME Ionophoresis and Electrostimulation Therapy
EME S.R.L.
EME Combine Electro and Ultrasound Therapy
EME S.R.L.
EME Ultrasound Therapy
EME S.R.L.
EME Combined Electro and Ultrasound Therapy Devices
EME S.R.L.
EME Shock Wave Therapy
EME SRL