BD Q-Syte™ Luer Access Split Septum - Indonesia BPOM Medical Device Registration
BD Q-Syte™ Luer Access Split Septum is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902614905. The device is manufactured by BECTON DICKINSON INFUSION THERAPY SYSTEMS INC. S.A. DE C.V. from Mexico, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BECTON DICKINSON INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
Mexico
Authorized Representative
PT. BECTON DICKINSON INDONESIAAR Address
Sampoerna Strategic Square South Tower 20th Floor Jl. Jend. Sudirman Kav 45-46
Registration Date
Aug 19, 2024
Expiry Date
Aug 25, 2026
Product Type
Therapeutic General and Individual Hospital Equipment
Intravascular catheter.
Non Electromedic Sterile
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