KADERMIN Powder Spray - Indonesia BPOM Medical Device Registration
KADERMIN Powder Spray is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603220740. The device is manufactured by PAVIA FARMACEUTICI S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TRITRA PRIMA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
PAVIA FARMACEUTICI S.R.L.Country of Origin
Italy
Authorized Representative
PT. TRITRA PRIMA INDONESIAAR Address
Central Park Cikarang Blok A1 No. 02
Registration Date
Nov 21, 2023
Expiry Date
Dec 31, 2026
Product Type
Surgical Equipment
Hydrogel wound dressing and burn dressing.
Non Electromedic Non Sterile
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