INTRAFIX® Safe Set for Gravity Infusion - Indonesia BPOM Medical Device Registration
INTRAFIX® Safe Set for Gravity Infusion is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902918388. The device is manufactured by B. BRAUN VIETNAM CO., LTD, from Vietnam, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is B. BRAUN MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
B. BRAUN VIETNAM CO., LTD,Country of Origin
Vietnam
Authorized Representative
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 25, 2022
Expiry Date
Jan 12, 2027
Product Type
Therapeutic General and Individual Hospital Equipment
Intravascular administration set
Non Electromedic Sterile
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