GBO ULTRATHERM 1008 - Indonesia BPOM Medical Device Registration
GBO ULTRATHERM 1008 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403901129. The device is manufactured by GBO MEDIZINTECHNIK AG. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. IT'S YOUR INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GBO MEDIZINTECHNIK AG.Country of Origin
Germany
Authorized Representative
PT. IT'S YOUR INDONESIAAR Address
Jl. Cideng Timur No.6B Jakarta Pusat 10130
Registration Date
Dec 07, 2020
Expiry Date
Dec 31, 2024
Product Type
Therapeutic Physical Health Equipment
Shortwave diathermy.
Non Radiation Electromedics
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