BOTTOM BOT - Indonesia BPOM Medical Device Registration
BOTTOM BOT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003420042. The device is manufactured by RED&BLUE CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ANDAMAN MEDICAL INDONESIA.
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PAIN BOT
Risk Classification
Product Class
Kelas : 2
Manufacturer
RED&BLUE CO., LTD.Country of Origin
Korea
Authorized Representative
PT. ANDAMAN MEDICAL INDONESIAAR Address
Menara Cardig Lantai 1, Jalan Raya Halim Perdanakusuma
Registration Date
May 07, 2024
Expiry Date
Dec 31, 2028
Product Type
Therapeutic Neurology Equipment
Transcutaneous electrical nerve stimulator for pain relief.
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