LYSIWAVE - Indonesia BPOM Medical Device Registration
LYSIWAVE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21604420032. The device is manufactured by BIOTEC ITALIA S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. HERCA CIPTA DERMAL PERDANA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BIOTEC ITALIA S.R.L.Country of Origin
Italy
Authorized Representative
PT. HERCA CIPTA DERMAL PERDANAAR Address
Taman Harapan Indah Blok FF 1 B No. 10 Kel. Jelambar Baru, Kec. Grogol Petamburan Jakarta Barat 11460
Registration Date
Aug 30, 2024
Expiry Date
Mar 22, 2027
Product Type
Therapeutic Surgical Equipment
Low Level Laser Systems for Aesthetic Use
Non Radiation Electromedics
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