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BIOLIGHT Fetal Monitor - Indonesia BPOM Medical Device Registration

BIOLIGHT Fetal Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21101420074. The device is manufactured by GUANGDONG BIOLIGHT MEDITECH. CO. LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GLOBAL MEDICAL PRESS.

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BPOM Registered
Risk Class Kelas Resiko : B
BIOLIGHT Fetal Monitor
Analysis ID: AKL 21101420074

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. GLOBAL MEDICAL PRESS

AR Address

Jl. Raya Kebon Jeruk No.26 RT.011 RW.002, Kelurahan Kebon Jeruk, Kecamatan Kebon Jeruk, Jakarta Barat, DKI Jakarta

Registration Date

Nov 18, 2024

Expiry Date

Dec 31, 2028

Product Type

Obstetric and Gynecological Monitoring Equipment

Fetal ultrasonic monitor and accessories.

Non Radiation Electromedics

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