PICOSURE Pro - Indonesia BPOM Medical Device Registration
PICOSURE Pro is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603420107. 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. IDS MEDICAL SYSTEMS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CYNOSURE, LLC.Country of Origin
United States
Authorized Representative
PT. IDS MEDICAL SYSTEMS INDONESIAAR Address
Gedung Wisma 76, Lantai 17 & 22, Jl. LetJend. S. Parman Kav.76, Kelurahan Slipi, Kecamatan Palmerah, 11410
Registration Date
Jan 17, 2024
Expiry Date
Dec 31, 2025
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
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