SKINMED PENTAGON - Indonesia BPOM Medical Device Registration
SKINMED PENTAGON is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603420728. The device is manufactured by BEIJING LEAD BEAUTY 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
BEIJING LEAD BEAUTY S&T CO., LTD.Country of Origin
China
Authorized Representative
PT. HERCA CIPTA DERMAL PERDANAAR Address
Taman Harapan Indah Blok FF 1 B No. 10 Kel. Jelambar Baru, Kec. Grogol Petamburan Jakarta Barat 11460
Registration Date
Apr 01, 2024
Expiry Date
Apr 01, 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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