SkinPen + SkinFuse Treatment Kit - Indonesia BPOM Medical Device Registration
SkinPen + SkinFuse Treatment Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603324633. The device is manufactured by CROWN AESTHETICS from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ANDAMAN MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
CROWN AESTHETICSCountry of Origin
United States
Authorized Representative
PT. ANDAMAN MEDICAL INDONESIAAR Address
Menara Cardig Lantai 1, Jalan Raya Halim Perdanakusuma
Registration Date
Aug 17, 2023
Expiry Date
Jan 01, 2028
Product Type
Surgical Equipment
Microneedling Device for Aesthetic Use
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