ARNEZ Fetal Monitor - Indonesia BPOM Medical Device Registration
ARNEZ Fetal Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21101420022. 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. SEKARGUNA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GUANGDONG BIOLIGHT MEDITECH CO., LTDCountry of Origin
China
Authorized Representative
PT. SEKARGUNA MEDIKAAR Address
JL. Ciputat Raya Nomor 64
Registration Date
Mar 22, 2024
Expiry Date
Mar 21, 2027
Product Type
Obstetric and Gynecological Monitoring Equipment
Fetal cardiac monitor.
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