VASOFIX Safety - Indonesia BPOM Medical Device Registration
VASOFIX Safety is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902011184. The device is manufactured by B. BRAUN MEDICAL INDUSTRIES SDN., BHD. from Malaysia, 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 INDUSTRIES SDN., BHD.Country of Origin
Malaysia
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
Feb 27, 2023
Expiry Date
Jan 12, 2027
Product Type
Therapeutic General and Individual Hospital Equipment
Intravascular catheter.
Non Electromedic Sterile
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