DIACAP Polysulfone - Indonesia BPOM Medical Device Registration
DIACAP Polysulfone is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805012291. The device is manufactured by B.BRAUN AVITUM SAXONIA GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. B BRAUN MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
B.BRAUN AVITUM SAXONIA GMBHCountry of Origin
Germany
Authorized Representative
PT. B BRAUN MEDICAL INDONESIAAR Address
Gedung Tempo Scan Tower Lt. 30 Jl. HR. Rasuna Said Kav. 3-4 RT.009 RW. 004 Kuningan Timur, Setiabudi Jakarta Selatan DKI Jakarta
Registration Date
Feb 04, 2019
Expiry Date
Nov 30, 2023
Product Type
Therapeutic Gastroenterology-Urology Equipment
Hemodialysis system and accessories.
Non Electromedic Sterile

