REMED Electromagnetic Stimulator - Indonesia BPOM Medical Device Registration
REMED Electromagnetic Stimulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003713845. The device is manufactured by REMED CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. NEURO MEDIKA SEJAHTERA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
REMED CO., LTD.Country of Origin
Korea
Authorized Representative
PT. NEURO MEDIKA SEJAHTERAAR Address
JL. PENJERNIHAN I NO.38
Registration Date
Jul 11, 2023
Expiry Date
Aug 13, 2024
Product Type
Therapeutic Neurology Equipment
Implanted peripheral nerve stimulator for pain relief.
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