BD Vacutainer K2 EDTA (K2E) - Indonesia BPOM Medical Device Registration
BD Vacutainer K2 EDTA (K2E) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101918810. The device is manufactured by BECTON, DICKINSON AND COMPANY. from United Kingdom, 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 Kingdom
Authorized Representative
PT. BECTON DICKINSON INDONESIAAR Address
Sampoerna Strategic Square South Tower 20th Floor, Jl. Jenderal Sudirman Kav. 45-46
Registration Date
Oct 20, 2021
Expiry Date
Nov 25, 2025
Product Type
Clinical Chemistry Test System
Blood specimen collection device
Invitro Diagnostics
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