BIONECT Crimea - Indonesia BPOM Medical Device Registration
BIONECT Crimea is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603601452. The device is manufactured by FIDIA FARMACEUTICI S.P.A. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is COMBIPHAR.
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BIONECT Krim
Risk Classification
Product Class
Kelas : 2
Manufacturer
FIDIA FARMACEUTICI S.P.A.Country of Origin
Italy
Authorized Representative
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 16, 2023
Expiry Date
Sep 05, 2028
Product Type
Surgical Equipment
Hydrogel wound dressing and burn dressing.
Non Electromedic Sterile
