BIONECT Gauze Pads - Indonesia BPOM Medical Device Registration
BIONECT Gauze Pads is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603910740. The device is manufactured by FIDIA FARMACEUTICI S.P.A. from Italy, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. COMBIPHAR.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
FIDIA FARMACEUTICI S.P.A.Country of Origin
Italy
Authorized Representative
PT. COMBIPHARAR Address
Gedung Office 8 Lt. 26, SCBD Lot 28, Jl. Jenderal Sudirman Kav. 52-53, Kode Pos 12190, Kel. Senayan, Kec. Kebayora Baru, Kota Jakarta Selatan, Prov. DKI Jakarta
Registration Date
Nov 08, 2023
Expiry Date
Sep 05, 2028
Product Type
Surgical Equipment
Nonresorbable gauze/sponge for external use, non sterile
Non Electromedic Sterile
