ARNEZ Finger Pulse Oximeter - Indonesia BPOM Medical Device Registration
ARNEZ Finger Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502420036. 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, LTD.Country of Origin
China
Authorized Representative
PT. SEKARGUNA MEDIKAAR Address
JL. Ciputat Raya Nomor 64
Registration Date
Jan 19, 2024
Expiry Date
Jan 18, 2027
Product Type
Monitoring Cardiology Equipment
Oximeter.
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