BISTOS Fetal Monitor - Indonesia BPOM Medical Device Registration
BISTOS Fetal Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21101520009. 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
Jan 17, 2025
Expiry Date
Apr 03, 2029
Product Type
Obstetric and Gynecological Monitoring Equipment
Fetal cardiac monitor.
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