DEYMED DuoMAG MP TMS System - Indonesia BPOM Medical Device Registration
DEYMED DuoMAG MP TMS System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003127757. The device is manufactured by DEYMED DIAGNOSTIC S.R.O from Czech Republic, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TIARA DATING.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DEYMED DIAGNOSTIC S.R.OCountry of Origin
Czech Republic
Authorized Representative
PT. TIARA DATINGAR Address
JL.RAYA PASAR MINGGU KM.18 NO.17
Registration Date
Oct 27, 2023
Expiry Date
Dec 31, 2027
Product Type
Therapeutic Neurology Equipment
Repetitive transcranial magnetic stimulation system
Non Radiation Electromedics
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