NEUROSOFT Repetitive Magnetic Stimulator - Indonesia BPOM Medical Device Registration
NEUROSOFT Repetitive Magnetic Stimulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003125315. The device is manufactured by NEUROSOFT LIMITED COMPANY. from Russian Federation, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. NEURO MEDIKA SEJAHTERA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
NEUROSOFT LIMITED COMPANY.Country of Origin
Russian Federation
Authorized Representative
PT. NEURO MEDIKA SEJAHTERAAR Address
JL. PENJERNIHAN I NO.38
Registration Date
Jul 12, 2022
Expiry Date
Dec 31, 2025
Product Type
Therapeutic Neurology Equipment
Repetitive transcranial magnetic stimulation system
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