LaserMe - Indonesia BPOM Medical Device Registration
LaserMe is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603520137. The device is manufactured by BERGER & KRAFT MEDICAL SP. ZO.O. from Poland, 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
BERGER & KRAFT MEDICAL SP. ZO.O.Country of Origin
Poland
Authorized Representative
PT. REGENESIS INDONESIAAR Address
Jalan Sultan Iskandar Muda No. 7 A dan B, Kebayoran lama Selatan, Kebayoran Lama, Jakarta Selatan
Registration Date
Jan 14, 2025
Expiry Date
Aug 29, 2027
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
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