B&E ELECTROLYTE CONTROL - Indonesia BPOM Medical Device Registration
B&E ELECTROLYTE CONTROL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101422542. The device is manufactured by B&E BIO-TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. WHIRA PITOE USAHABERSAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
B&E BIO-TECHNOLOGY CO., LTD.Country of Origin
China
Authorized Representative
PT. WHIRA PITOE USAHABERSAMAAR Address
Ruko Buaran Persada NO. 10, Jl. Jend. R.S. Soekanto RT.008 RW.006
Registration Date
Dec 16, 2024
Expiry Date
May 12, 2027
Product Type
Clinical Chemistry Test System
Quality control material (assayed and unassayed) (cair)
Invitro Diagnostics
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