LKTECH Diode Laser - Indonesia BPOM Medical Device Registration
LKTECH Diode Laser is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21604320039. The device is manufactured by BEIJING SANO LASER S&T DEVELOPMENT, CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. JAMBERDETAK DERMA TECH.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BEIJING SANO LASER S&T DEVELOPMENT, CO., LTD.Country of Origin
China
Authorized Representative
PT. JAMBERDETAK DERMA TECHAR Address
KOMPLEK PAKUAN, Jl. INTAN PAKUAN II NOMOR 2, RT 002 RW 007
Registration Date
Sep 04, 2023
Expiry Date
Sep 01, 2026
Product Type
Therapeutic Surgical Equipment
Low Level Laser Systems for Aesthetic Use
Non Radiation Electromedics
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