BD Ultra-Fine ™ PRO - Indonesia BPOM Medical Device Registration
BD Ultra-Fine ™ PRO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902420298. The device is manufactured by BECTON DICKINSON AND COMPANY from Ireland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BRIDGE TWO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BECTON DICKINSON AND COMPANYCountry of Origin
Ireland
Authorized Representative
PT. BRIDGE TWOAR Address
Jl. Petojo Melintang No. 17
Registration Date
May 21, 2024
Expiry Date
Jan 03, 2029
Product Type
Therapeutic General and Individual Hospital Equipment
Hypodermic single lumen needle.
Non Electromedic Sterile
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