LUMENIS Pulse 100H - Indonesia BPOM Medical Device Registration
LUMENIS Pulse 100H is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603222509. The device is manufactured by LUMENIS LTD. from Israel, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SURGIKA ALKESINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LUMENIS LTD.Country of Origin
Israel
Authorized Representative
PT. SURGIKA ALKESINDOAR Address
Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih
Registration Date
Jul 09, 2024
Expiry Date
Sep 30, 2025
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
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