BISTOS Patient Monitor - Indonesia BPOM Medical Device Registration
BISTOS Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502220066. The device is manufactured by BISTOS CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MEGA PRATAMA MEDICALINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BISTOS CO., LTD.Country of Origin
Korea
Authorized Representative
MEGA PRATAMA MEDICALINDOAR Address
Jl. Pluit Raya 133 Blok A.3
Registration Date
Mar 09, 2022
Expiry Date
Dec 23, 2026
Product Type
Monitoring Cardiology Equipment
Cardiac monitor (including cardiotachometer and rate alarm).
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