BD BACTEC MGIT 960 PZA Medium - Indonesia BPOM Medical Device Registration
BD BACTEC MGIT 960 PZA Medium is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20301715396. The device is manufactured by BECTON, DICKINSON AND COMPANY. 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
BECTON, DICKINSON AND COMPANY.Country of Origin
United States
Authorized Representative
PT. BECTON DICKINSON INDONESIAAR Address
Sampoerna Strategic Square South Tower 20th Floor Jl. Jend. Sudirman Kav 45-46
Registration Date
Sep 27, 2024
Expiry Date
Dec 21, 2028
Product Type
Diagnostic Equipment
Antimicrobial susceptibility test powder.
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