PLASMAGE - Indonesia BPOM Medical Device Registration
PLASMAGE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603520016. The device is manufactured by BRERA MEDICAL TECHNOLOGIES S.R.L from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is SURGIKA ALKESINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BRERA MEDICAL TECHNOLOGIES S.R.LCountry of Origin
Italy
Authorized Representative
SURGIKA ALKESINDOAR Address
Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih
Registration Date
Jan 03, 2025
Expiry Date
Aug 11, 2026
Product Type
Surgical Equipment
Electrosurgical device for over-the-counter aesthetic use
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