B. Braun Celsite Safety - Indonesia BPOM Medical Device Registration
B. Braun Celsite Safety is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501420476. The device is manufactured by B. BRAUN MEDICAL from France, 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 MEDICALCountry of Origin
France
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
Oct 11, 2024
Expiry Date
May 29, 2029
Product Type
Diagnostic Cardiology Equipment
Diagnostic intravascular catheter.
Non Electromedic Sterile
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