NEUROSOFT Transcranial Electrical Stimulator - Indonesia BPOM Medical Device Registration
NEUROSOFT Transcranial Electrical Stimulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003520001. The device is manufactured by NEUROSOFT, LLC from Russia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is NEURO MEDIKA SEJAHTERA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
NEUROSOFT, LLCCountry of Origin
Russia
Authorized Representative
NEURO MEDIKA SEJAHTERAAR Address
Bersaudara Building Lt. 3, Jl Penjernihan 1 No. 38 RT.002/RW.008.
Registration Date
Jan 04, 2025
Expiry Date
Dec 31, 2025
Product Type
Therapeutic Neurology Equipment
Cranial electrotheraphy stimulator.
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