ENDYMED Pure Laser - Indonesia BPOM Medical Device Registration
ENDYMED Pure Laser is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603422629. The device is manufactured by ENDYMED ASIA LIMITED from Hong Kong (China), and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. REDO MARKETING INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ENDYMED ASIA LIMITEDCountry of Origin
Hong Kong (China)
Authorized Representative
PT. REDO MARKETING INDONESIAAR Address
Ruko Renata Jl.Jalur Sutera Timur Blok 1A No. 9 Alam Sutera Kel. Kunciran Kec. Pinang
Registration Date
Nov 11, 2024
Expiry Date
Jul 12, 2027
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
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