AUTOCHECK Glucare Glucose Control Solution - Indonesia BPOM Medical Device Registration
AUTOCHECK Glucare Glucose Control Solution is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101025060. The device is manufactured by I-SENS, INC. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEGA PRATAMA MEDICALINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
I-SENS, INC.Country of Origin
Korea
Authorized Representative
PT. MEGA PRATAMA MEDICALINDOAR Address
Jl. Pluit Raya 133 Blok A.3
Registration Date
Apr 10, 2023
Expiry Date
Mar 13, 2026
Product Type
Clinical Chemistry Test System
Quality control material (assayed and unassayed) (cair)
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