MONALISA Lidocaine Filler - Indonesia BPOM Medical Device Registration
MONALISA Lidocaine Filler is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602320321. The device is manufactured by GENOSS CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. ICT WORLDWIDE INDONESIA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
GENOSS CO., LTDCountry of Origin
Korea
Authorized Representative
PT. ICT WORLDWIDE INDONESIAAR Address
Gedung Annex RS Jakarta Lt. 3, Jl. Jenderal Sudirman Kav. 49, Kel. Karet Semanggi, Kec. Setiabudi, Kota Adm. Jakarta Selatan, Provinsi DKI Jakarta, Kode Pos 12930
Registration Date
Dec 19, 2023
Expiry Date
Mar 31, 2028
Product Type
Prosthetic Surgical Equipment
Dermal filler
Non Electromedic Sterile
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