INFUSOMAT Plus Line - Indonesia BPOM Medical Device Registration
INFUSOMAT Plus Line is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902121615. The device is manufactured by B. BRAUN MEDICAL KFT. PRODUCTION DIVISION from Hungary, 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 MEDICAL KFT. PRODUCTION DIVISIONCountry of Origin
Hungary
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
Sep 17, 2024
Expiry Date
Apr 03, 2029
Product Type
Therapeutic General and Individual Hospital Equipment
Intravascular administration set
Non Electromedic Sterile
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