SKINMED® HEALIGHT - Indonesia BPOM Medical Device Registration
SKINMED® HEALIGHT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403320692. The device is manufactured by BEIJING LEAD BEAUTY S&T CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is HERCA CIPTA DERMAL PERDANA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BEIJING LEAD BEAUTY S&T CO., LTDCountry of Origin
China
Authorized Representative
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
Aug 01, 2023
Expiry Date
Dec 08, 2027
Product Type
Therapeutic Physical Health Equipment
Infrared lamp.
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