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 20502913277. 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 no 14 B.Pondok Pinang
Registration Date
Apr 13, 2022
Expiry Date
Nov 26, 2023
Product Type
Monitoring Cardiology Equipment
Oximeter.
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