LKTECH IPL - Indonesia BPOM Medical Device Registration
LKTECH IPL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603421182. The device is manufactured by BEIJING KES BIOLOGY TECHNOLOGY 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 KES BIOLOGY TECHNOLOGY CO., LTDCountry of Origin
China
Authorized Representative
PT. JAMBERDETAK DERMA TECHAR Address
KOMPLEK PAKUAN, Jl. INTAN PAKUAN II NOMOR 2, RT 002 RW 007
Registration Date
Jun 03, 2024
Expiry Date
Jun 03, 2027
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
Non Radiation Electromedics
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LKTECH PICO PRIME MAXIMUS
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LKTECH CO2 Fractional Laser System
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