BD VENFLON™ - Indonesia BPOM Medical Device Registration
BD VENFLON™ is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902614533. The device is manufactured by BECTON DICKINSON INDIA PVT., LTD. from India, 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
Manufacturer
BECTON DICKINSON INDIA PVT., LTD.Country of Origin
India
Authorized Representative
PT. BECTON DICKINSON INDONESIAAR Address
Sampoerna Strategic Square South Tower 20th Floor Jl. Jend. Sudirman Kav 45-46
Registration Date
Aug 04, 2024
Expiry Date
Apr 07, 2026
Product Type
Therapeutic General and Individual Hospital Equipment
Intravascular catheter.
Non Electromedic Sterile
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