JUVELOOK Volume - Indonesia BPOM Medical Device Registration
JUVELOOK Volume is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602420173. The device is manufactured by SPIRIT 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
SPIRIT CO., LTDCountry 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
Dec 23, 2024
Expiry Date
Mar 14, 2029
Product Type
Prosthetic Surgical Equipment
Dermal filler
Non Electromedic Sterile
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