BD VENFLON ™ Pro Safety - Indonesia BPOM Medical Device Registration
BD VENFLON ™ Pro Safety is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902121440. The device is manufactured by BECTON DICKINSON MEDICAL(S) PTE LTD from Singapore, 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 MEDICAL(S) PTE LTDCountry of Origin
Singapore
Authorized Representative
PT. BECTON DICKINSON INDONESIAAR Address
Sampoerna Strategic Square South Tower 20th Floor Jl. Jend. Sudirman Kav 45-46
Registration Date
Jul 31, 2024
Expiry Date
Jan 20, 2026
Product Type
Therapeutic General and Individual Hospital Equipment
Intravascular catheter.
Non Electromedic Sterile
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