Pulsed Magnetic Stimulation Device - Indonesia BPOM Medical Device Registration
Pulsed Magnetic Stimulation Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003320157. The device is manufactured by SHENZHEN YINGCHI TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PETAN DAYA MEDICA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHENZHEN YINGCHI TECHNOLOGY CO., LTDCountry of Origin
China
Authorized Representative
PETAN DAYA MEDICAAR Address
Komplek Setia Budi Point Jl. Setia Budi Blok C No. 3-4 Medan
Registration Date
Sep 18, 2023
Expiry Date
Dec 31, 2025
Product Type
Therapeutic Neurology Equipment
Repetitive transcranial magnetic stimulation system
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