FEMILIFT ALMA Laser Surgical System - Indonesia BPOM Medical Device Registration
FEMILIFT ALMA Laser Surgical System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603711522. The device is manufactured by ALMA LASER LTD. 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 LASER LTD.Country of Origin
Germany
Authorized Representative
PT. REGENESIS INDONESIAAR Address
Jl. Sultan Iskandar Muda No. 7A & B
Registration Date
Jun 14, 2021
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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