Rigeneracons tube/ devices - Indonesia BPOM Medical Device Registration
Rigeneracons tube/ devices is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203026071. The device is manufactured by HUMAN BRAIN WAVE SRL from Italy, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. REGENESIS INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
HUMAN BRAIN WAVE SRLCountry of Origin
Italy
Authorized Representative
PT. REGENESIS INDONESIAAR Address
Jalan Sultan Iskandar Muda No. 7 A dan B, Kebayoran lama Selatan, Kebayoran Lama, Jakarta Selatan
Registration Date
Oct 13, 2024
Expiry Date
Jul 08, 2025
Product Type
Pathology Equipment and Accessories
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