STICOL Volume - Indonesia BPOM Medical Device Registration
STICOL Volume is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602420103. The device is manufactured by PRP SCIENCE CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. HAJU MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
PRP SCIENCE CO., LTD.Country of Origin
Korea
Authorized Representative
PT. HAJU MEDICAL INDONESIAAR Address
Gedung Tifa Arum Realty Lt.8, Suite 801 Jl. Kuningan Barat 1 No. 26, Kelurahan Kuningan Barat, Kecamatan Mampang Prapatan. Jakarta Selatan, DKI Jakarta
Registration Date
Aug 12, 2024
Expiry Date
Apr 19, 2029
Product Type
Prosthetic Surgical Equipment
Dermal filler
Non Electromedic Sterile
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