BIOLYTE 2000 Reagent Pack With Septum - Indonesia BPOM Medical Device Registration
BIOLYTE 2000 Reagent Pack With Septum is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101120139. The device is manufactured by BIOCARE CORPORATION from Taiwan (China), and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TAMARA OVERSEAS CORPORINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BIOCARE CORPORATIONCountry of Origin
Taiwan (China)
Authorized Representative
PT. TAMARA OVERSEAS CORPORINDOAR Address
Jl. Pinangsia Timur No. 49 Jakarta 11110
Registration Date
Jan 07, 2021
Expiry Date
Jun 22, 2025
Product Type
Clinical Chemistry Test System
Multi parameter clinical chemistry test system
Invitro Diagnostics
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BIOCARE Biolyte ™ 2000 Reference ISE / Ref ISE
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