BD Filter Needle - Indonesia BPOM Medical Device Registration
BD Filter Needle is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902711193. The device is manufactured by BD MEDICAL SURGICAL SYSTEM from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BECTON DICKINSON INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BD MEDICAL SURGICAL SYSTEMCountry of Origin
United States
Authorized Representative
PT. BECTON DICKINSON INDONESIAAR Address
Sampoerna Strategic Square South Tower 20th Floor, Jl. Jenderal Sudirman Kav. 45-46
Registration Date
Jul 07, 2022
Expiry Date
Feb 15, 2027
Product Type
Therapeutic General and Individual Hospital Equipment
Hypodermic single lumen needle.
Non Electromedic Sterile
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