MIFILL Volume Plus Lidocaine - Indonesia BPOM Medical Device Registration
MIFILL Volume Plus Lidocaine is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602220061. The device is manufactured by BIOPLUS 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
BIOPLUS 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
Jul 10, 2023
Expiry Date
May 26, 2026
Product Type
Prosthetic Surgical Equipment
Dermal filler
Non Electromedic Sterile
LUMIGLAM S
LUMIGLAM H
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