FINEBEAM Dual - Indonesia BPOM Medical Device Registration
FINEBEAM Dual is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603022990. The device is manufactured by SNJ CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. HAJU MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SNJ CO., LTD.Country of Origin
Korea
Authorized Representative
PT. HAJU MEDICAL INDONESIAAR Address
Gedung Tifa Arum Realty Lantai 8 Suite 801 dan Lantai Annex Timur Suite Annex 03, Jl. Kuningan Barat I No. 26
Registration Date
Jan 15, 2025
Expiry Date
Nov 18, 2029
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
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