EME Diathermy Therapy - Indonesia BPOM Medical Device Registration
EME Diathermy Therapy is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403125104. The device is manufactured by EME SRL 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 SRLCountry of Origin
Italy
Authorized Representative
AGINTA SURGICALINDOAR Address
Ruko Grand Pasar Minggu Jl. Rawa Bambu No. 88 R
Registration Date
Dec 02, 2023
Expiry Date
Dec 31, 2025
Product Type
Therapeutic Physical Health Equipment
Ultrasonic diathermy.
Non Radiation Electromedics
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