DERMALAX™ PLUS - Indonesia BPOM Medical Device Registration
DERMALAX™ PLUS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602220012. The device is manufactured by ACROSS CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. HERCA CIPTA DERMAL PERDANA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
ACROSS CO., LTDCountry of Origin
Korea
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
Jan 26, 2022
Expiry Date
Jul 23, 2024
Product Type
Prosthetic Surgical Equipment
Dermal filler
Non Electromedic Sterile
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