LIPOLIFE - Indonesia BPOM Medical Device Registration
LIPOLIFE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603715418. The device is manufactured by ALMA LASERS from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. REGENESIS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ALMA LASERSCountry of Origin
Germany
Authorized Representative
PT. REGENESIS INDONESIAAR Address
Jl. Sultan Iskandar Muda No. 7A & B
Registration Date
Jan 20, 2022
Expiry Date
Mar 17, 2026
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
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