PERFECTHA FINELINES - Indonesia BPOM Medical Device Registration
PERFECTHA FINELINES is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602320141. The device is manufactured by SINCLAIR FRANCE SAS from France, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is BINASUKSES CANTEEN.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
SINCLAIR FRANCE SASCountry of Origin
France
Authorized Representative
BINASUKSES CANTEENAR Address
JL. PULO KAMBING II NO.26 KAWASAN INDUSTRI PULOGADUNG
Registration Date
Feb 01, 2023
Expiry Date
Jan 20, 2026
Product Type
Prosthetic Surgical Equipment
Dermal filler
Non Electromedic Sterile
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