BD BBL™ Salmonella Shigella Agar - Indonesia BPOM Medical Device Registration
BD BBL™ Salmonella Shigella Agar is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10302717592. The device is manufactured by BECTON, DICKINSON AND COMPANY (39L) from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BECTON DICKINSON INDONESIA.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 1
Manufacturer
BECTON, DICKINSON AND COMPANY (39L)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
Jan 20, 2025
Expiry Date
Dec 20, 2028
Product Type
Microbiology Equipment
Selective culture medium.
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