CFU Elife - Indonesia BPOM Medical Device Registration
CFU Elife is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603324181. The device is manufactured by BIOTEC ITALIA S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. OPTIMA DERMA TECH.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BIOTEC ITALIA S.R.L.Country of Origin
Italy
Authorized Representative
PT. OPTIMA DERMA TECHAR Address
JALAN KEBON JERUK RAYA 3a (GEDUNG Q-DERMA), Lantai 4
Registration Date
Dec 04, 2023
Expiry Date
Dec 31, 2024
Product Type
Surgical Equipment
Focused ultrasound stimulator system for aesthetic use
Non Radiation Electromedics

