PAIN BLOCK - Indonesia BPOM Medical Device Registration
PAIN BLOCK is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003022837. The device is manufactured by KOIBIG CO. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KMD INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
KOIBIG CO.Country of Origin
Korea
Authorized Representative
PT. KMD INDONESIAAR Address
Menara Palma lantai 7-06B, Jl. HR. Rasuna Said, Blok X2 Kav. 6
Registration Date
May 19, 2020
Expiry Date
Jan 02, 2025
Product Type
Therapeutic Neurology Equipment
Transcutaneous electrical nerve stimulator for pain relief.
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