RENAFLO II Hemofilter - Indonesia BPOM Medical Device Registration
RENAFLO II Hemofilter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805615421. The device is manufactured by MEDIVATORS INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. REKAMILENIUMINDO SELARAS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MEDIVATORS INC.Country of Origin
United States
Authorized Representative
PT. REKAMILENIUMINDO SELARASAR Address
Jl. Tomang Raya No. 51B RT 01 RW 05, Kelurahan Tomang
Registration Date
Sep 13, 2023
Expiry Date
Dec 31, 2026
Product Type
Therapeutic Gastroenterology-Urology Equipment
High permeability hemodialysis system.
Non Electromedic Sterile
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