FLIXENE Vascular Graft - Indonesia BPOM Medical Device Registration
FLIXENE Vascular Graft is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20503811243. The device is manufactured by ATRIUM MEDICAL CORPORATION from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is MAGENTA BIOMEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ATRIUM MEDICAL CORPORATIONCountry of Origin
United States
Authorized Representative
MAGENTA BIOMEDIKAAR Address
Ruko Buaran Persada No. 30, Jl. Raya Soekamto, Duren Sawit
Registration Date
Dec 07, 2023
Expiry Date
Dec 31, 2025
Product Type
Prosthetic Cardiology Equipment
Vascular graft prosthesis.
Non Electromedic Sterile

