SKINMED TRILASE LASER - Indonesia BPOM Medical Device Registration
SKINMED TRILASE LASER is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603422673. The device is manufactured by NANJING BESTVIEW LASER S&T CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. HERCA CIPTA DERMAL PERDANA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
NANJING BESTVIEW LASER S&T CO., LTD.Country of Origin
China
Authorized Representative
PT. HERCA CIPTA DERMAL PERDANAAR Address
TAMAN HARAPAN INDAH BLOK FF I-B NO.10 RT. 014 RW.007
Registration Date
Nov 18, 2024
Expiry Date
Nov 18, 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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