MR Electromagnetic Stimulator - Indonesia BPOM Medical Device Registration
MR Electromagnetic Stimulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003320164. The device is manufactured by MEDICAL REVOLUTION / MR. INC. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MAIN MEDICAL PARTNERS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MEDICAL REVOLUTION / MR. INC.Country of Origin
Korea
Authorized Representative
PT. MAIN MEDICAL PARTNERSAR Address
JL. DR. Wahidin No 68 D,
Registration Date
Sep 10, 2023
Expiry Date
Jun 21, 2028
Product Type
Therapeutic Neurology Equipment
Transcutaneous electrical nerve stimulator for pain relief.
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