B. BRAUN Omnifix Single Use Syringe Without Needle - Indonesia BPOM Medical Device Registration
B. BRAUN Omnifix Single Use Syringe Without Needle is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902600243. The device is manufactured by B. BRAUN MEDICAL AG. from Switzerland, and is classified as Risk Class Kelas Resiko : B. 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 AG.Country of Origin
Switzerland
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
Dec 12, 2022
Expiry Date
Jan 12, 2027
Product Type
Therapeutic General and Individual Hospital Equipment
Piston syringe.
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