CYNERGY - Indonesia BPOM Medical Device Registration
CYNERGY is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603614568. The device is manufactured by CYNOSURE, INC. 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, INC.Country of Origin
United States
Authorized Representative
PT. MEDIVAAR Address
K-LINK TOWER, LEVEL 11, SUITE G. JL. Jend. Gatot Subroto Kav. 59A
Registration Date
Jan 01, 2022
Expiry Date
Jun 30, 2024
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
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