Regenerate Machine - Indonesia BPOM Medical Device Registration
Regenerate Machine is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203025959. 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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Rigenera Machine
Risk Classification
Product Class
Kelas : 1
Manufacturer
HUMAN BRAIN WAVE SRLCountry of Origin
Italy
Authorized Representative
PT. REGENESIS INDONESIAAR Address
Jl. Panglima Polim Raya Blok B III/107, Jakarta Selatan
Registration Date
Oct 07, 2020
Expiry Date
Jul 08, 2025
Product Type
Pathology Equipment and Accessories
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