HYALONE - Indonesia BPOM Medical Device Registration
HYALONE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31302511695. The device is manufactured by FIDIA FARMACEUTICI S.P.A. from Italy, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. COMBIPHAR.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
FIDIA FARMACEUTICI S.P.A.Country of Origin
Italy
Authorized Representative
PT. COMBIPHARAR Address
Gedung Office 8 Lt.26, SCBD Lot 28, Jl Jend. Sudirman Kav. 52-53
Registration Date
Dec 31, 2024
Expiry Date
Sep 05, 2028
Product Type
Prosthetic Orthopedic Equipment
Intra articular fluid
Non Electromedic Sterile
