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MEDIAN Fetal Monitor - Indonesia BPOM Medical Device Registration

MEDIAN Fetal Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21101320069. 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 PT. DEMKA SAKTI.

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Risk Class Kelas Resiko : B
MEDIAN Fetal Monitor

MEDIANA Fetal Monitor

Analysis ID: AKL 21101320069

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

BISTOS CO.,LTD

Country of Origin

Korea

Authorized Representative

PT. DEMKA SAKTI

AR Address

Jl. Tanah Abang III No. 19 A - B, Jakarta Pusat

Registration Date

Feb 07, 2023

Expiry Date

Jul 31, 2025

Product Type

Obstetric and Gynecological Monitoring Equipment

Fetal ultrasonic monitor and accessories.

Non Radiation Electromedics

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