ARNEZ Pulse Oximeter 2 in 1 - Indonesia BPOM Medical Device Registration
ARNEZ Pulse Oximeter 2 in 1 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502911048. 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
Nov 08, 2023
Expiry Date
Nov 07, 2026
Product Type
Monitoring Cardiology Equipment
Oximeter.
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