BD PLASTIPAK โข Syringe 50 ml - Indonesia BPOM Medical Device Registration
BD PLASTIPAK โข Syringe 50 ml is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902220480. The device is manufactured by BECTON DICKINSON S.A. from Spain, 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 S.A.Country of Origin
Spain
Authorized Representative
PT. BECTON DICKINSON INDONESIAAR Address
Sampoerna Strategic Square South Tower 20th Floor Jl. Jend. Sudirman Kav 45-46
Registration Date
Sep 26, 2024
Expiry Date
Sep 14, 2026
Product Type
Therapeutic General and Individual Hospital Equipment
Piston syringe.
Non Electromedic Sterile
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