PICOSURE - Indonesia BPOM Medical Device Registration
PICOSURE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603614009. The device is manufactured by CYNOSURE LLC from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDIVA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CYNOSURE LLCCountry of Origin
United States
Authorized Representative
PT. MEDIVAAR Address
K-LINK TOWER, LEVEL 11, SUITE G. JL. Jend. Gatot Subroto Kav. 59A
Registration Date
Mar 25, 2022
Expiry Date
Jun 30, 2024
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
Non Radiation Electromedics
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