DIACAP PRO - Indonesia BPOM Medical Device Registration
DIACAP PRO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805711927. 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 Lantai 30, Jl. HR Rasuna Said Kav. 3-4 RT 009 RW 004 Kel. Kuningan Timur, Kec. Setiabudi, Kota Administrasi Jakarta Selatan
Registration Date
Nov 16, 2022
Expiry Date
Jan 15, 2026
Product Type
Therapeutic Gastroenterology-Urology Equipment
High permeability hemodialysis system.
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