SKINMED® SCARLUX - Indonesia BPOM Medical Device Registration
SKINMED® SCARLUX is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603421300. 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 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
Jun 20, 2024
Expiry Date
Dec 08, 2025
Product Type
Surgical Equipment
Microneedling Device for Aesthetic Use
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